Intravascular treatment of vascular occlusion and associated devices, systems, and methods

ABSTRACT

Systems and methods for removal of thrombus from a blood vessel in a body of a patient are disclosed herein. The method can include: providing a thrombus extraction device including a proximal self-expanding member formed of a unitary fenestrated structure, a distal substantially cylindrical portion formed of a net-like filament mesh structure, and an inner shaft member connected to a distal end of the net-like filament mesh structure; advancing a catheter constraining the thrombus extraction device through a vascular thrombus, deploying the thrombus extraction; retracting the thrombus extraction device to separate a portion of the thrombus from the vessel wall and to capture the portion of the thrombus within the net-like filament mesh structure; and withdrawing the thrombus extraction device from the body to remove thrombus from the patient.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation of U.S. Pat. Application No.17/362,800, filed Jun. 29, 2021, which is a continuation of U.S. Pat.Application No. 16/425,017, filed May 29, 2019, issued as U.S. Pat. No.11,058,451, which is a divisional of U.S. Pat. Application No.15/268,406, filed Sep. 16, 2016, issued as U.S. Pat. No. 10,342,571,which is a continuation of U.S. Pat. Application No. 15/268,296, filedSep. 16, 2016, issued as U.S. Pat. No. 9,700,332, which claims thebenefit of U.S. Provisional Pat. Application No. 62/245,935, filed onOct. 23, 2015, each of which is herein incorporated by reference in itsentirety.

BACKGROUND OF THE INVENTION

Thrombosis is a term for a blood clot occurring inside a blood vessel,and a venous thrombus is a blood clot (thrombus) that forms within avein. A common type of venous thrombosis is a deep vein thrombosis(DVT). DVT is the formation of a blood clot (thrombus) within a deepvein, predominantly in the legs. Nonspecific signs may include pain,swelling, redness, warmness, and engorged superficial veins.

If the thrombus breaks off (embolizes) and flows towards the lungs, itcan become a life-threatening pulmonary embolism (PE), a blood clot inthe lungs. In addition to the loss of life that can arise from PE, DVTcan cause significant health issues such as post thrombotic syndrome,which can cause chronic swelling, pressure, pain, and ulcers due tovalve and vessel damage. Further, DVT can result in significanthealth-care costs either directly or indirectly through the treatment ofrelated complications and inability of patients to work.

Three processes are believed to result in venous thrombosis. These are adecreased blood flow rate (venous stasis), increased tendency to clot(hypercoagulability), and changes to the blood vessel wall. DVTformation typically begins inside the valves of the calf veins, wherethe blood is relatively oxygen deprived, which activates certainbiochemical pathways. Several medical conditions increase the risk forDVT, including diabetes, cancer, trauma, and antiphospholipid syndrome.Other risk factors include older age, surgery, immobilization (as withbed rest, orthopedic casts, and sitting on long flights), combined oralcontraceptives, pregnancy, the postnatal period, and genetic factors.The rate of DVT increases dramatically from childhood to old age and inadulthood, about 1 in 1,000 adults develops it annually.

While current devices and methods of prevention and/or treatment of DVTexist, there are a number of shortcomings that have yet to be resolved,such as high incidence of DVT re-occurrence, use of devices not designedto remove large clot volumes, and/or complicated treatments involvingmultiple treatment devices and/or pharmaceuticals. Accordingly, newdevices, systems, and methods of treating thrombus, and particularly DVTare desired.

BRIEF SUMMARY OF THE INVENTION

Aspects of the present disclosure relate to systems and methods forthrombus extraction, and particularly for thrombus extraction from aperipheral vasculature. The thrombus extraction devices of the presentinvention are designed to remove large clot volumes, including matureand organized clots, with reduced needs for pharmaceuticals, such asthrombolytics. This reduces risk of bleeding, post-treatment recoverytime, and reduces health care procedure costs. The thrombus extractiondevice may comprise a self-expanding coring portion connected to abraided net so as to effectively core and separate large volumes ofthrombus from large vessels in, for example, the venous system orarterial system while capturing the separated thrombus in the braidednet.

In some embodiments, the thrombus can be extracted via the use of athrombectomy system including an introducer sheath having aself-expanding funnel and a thrombus extraction catheter including athrombus extraction device. The thrombus extraction device can include aself-expanding coring portion that can be a stent portion and anexpandable cylindrical portion that can be a braided filament mesh. Theexpandable cylindrical portion can be formed onto a distal end of theself-expanding coring portion so as to form a unitary thrombusextraction device. In some embodiments, the coring element may have asharp cutting edge to further enhance its ability to detach thrombusfrom the vessel wall.

One aspect of the present disclosure relates to a method of treatingdeep vein thrombosis in a peripheral vasculature of a patient. Themethod includes providing a thrombus extraction device including aproximal self-expanding coring portion, which can be a stent, formed ofa unitary fenestrated structure and a distal expandable cylindricalportion, that can be tubular, formed of a braided filament meshstructure. In some embodiments, the mesh structure is integrally formedwith the fenestrated structure so that a proximal end of the meshstructure is attached to a distal end of the fenestrated structure. Themethod includes advancing a catheter constraining the thrombusextraction device through a vascular thrombus in a venous vessel. Insome embodiments, an intermediate shaft slidably extends through thecatheter and a distal end thereof is coupled to a proximal end of thefenestrated structure. In some embodiments, an inner shaft slidablyextends through the intermediate shaft and a distal end thereof iscoupled to a distal end of the mesh structure. The method includesdeploying the thrombus extraction device from the catheter from aconstrained configuration to an expanded configuration. In someembodiments, the thrombus extraction device engages at least a wall ofthe venous vessel distally past a portion of the vascular thrombus atfull expansion. The method includes retracting the thrombus extractiondevice proximally so that the coring portion cores and separates aportion of the vascular thrombus from the venous vessel wall while themesh structure captures the vascular thrombus portion. The methodincludes withdrawing the thrombus extraction device from the patient toremove the vascular thrombus portion from the venous vessel.

In some embodiments, advancing the catheter includes inserting thecatheter into the venous vessel until a radiopaque distal tip of thecatheter is distally past the vascular thrombus portion. In someembodiments, deploying the thrombus extraction device from the catheterfrom the constrained configuration to the expanded configurationincludes advancing the intermediate shaft distally until the coringportion of the thrombus extraction device is beyond a distal end of thecatheter.

In some embodiments, deploying the thrombus extraction device furtherincludes: locking the intermediate shaft with respect to the catheter;retracting the inner shaft with respect to the catheter and theintermediate shaft until a stop feature fixed on the inner shaft engagesa corresponding feature on the stent portion slidably connected to theinner shaft for full expansion of the thrombus extraction device, whichstent portion maintains sufficient radial force on the venous vesselwall to core and separate the vascular thrombus portion at fullexpansion; and dynamically coupling the inner shaft with respect to theintermediate shaft. In some embodiments, the coring portion has a coringangle between 30 degrees and 45 degrees when the thrombus extractiondevice is at full expansion. In some embodiments, deploying the thrombusextraction device further includes determining a position of thethrombus extraction device with respect to the catheter via imaging of afirst radiopaque marker located on the catheter and a second radiopaquemarker located on at least one of the intermediate shaft, the innershaft, stent portion, or mesh structure.

In some embodiments, the vascular thrombus portion is captured into themesh structure by entering the expandable tubular portion and/orcylindrical portion via at least opening or aperture located at theproximal end of the self-expanding stent portion. In some embodiments,the method includes inserting the catheter into the venous vesselthrough an access site, which access site is a popliteal access site, afemoral access site, or an internal jugular access site. In someembodiments, the venous vessel has a diameter of at least 5 millimetersand is at least one of a femoral vein, an iliac vein, a popliteal vein,a posterior tibial vein, an anterior tibial vein, or a peroneal vein.

In some embodiments the method further includes: percutaneouslyaccessing the venous vessel of the patient with an introducer sheaththrough an access site into the venous vessel of the patient; advancinga distal end of the introducer sheath to a position proximal of thevascular thrombus; deploying a self-expanding funnel on the distal endof the introducer sheath; and inserting the catheter through a lumen ofthe introducer sheath so that a distal tip of the catheter is distallypast the vascular thrombus portion. In some embodiments, deploying theself-expanding funnel includes: advancing an obturator having a capturesheath feature on a distal end thereof to unsheathe the self-expandingfunnel from a constrained configuration within the capture sheathfeature to a deployed configuration free of the capture sheath feature;and removing the obturator from the introducer sheath by retracting theobturator through or outside the deployed self-expanding funnel andthrough or outside the lumen of the introducer sheath. In someembodiments, withdrawing the thrombus extraction device from the patientincludes: retracting the thrombus extraction device relative to theintroducer sheath until an opening of the self-expanding stent portionis within the self-expanding funnel; collapsing the stent portion andmesh structure so as to compress the vascular thrombus portion therein;retracting the stent portion and mesh structure into the introducersheath; and removing the thrombus extraction device from the introducersheath.

In some embodiments the method further includes extruding at least someof the vascular thrombus portion through pores located at a distalportion of the expandable tubular portion and/or cylindrical portion andcapturing a part of the at least some of the vascular thrombus portionin the self-expanding funnel or further compressing the at least onepiece of the vascular thrombus portion through a mesh of theself-expanding funnel. In some embodiments the method further includesaspirating at least one piece of the vascular thrombus portion remainingwithin the self-expanding funnel from the venous vessel and through anaspiration port connected to a proximal end of the introducer sheath.

In some embodiments the method further includes verifying that theopening of the self-expanding stent portion is within the self-expandingfunnel via fluoroscopy prior to collapsing the stent portion and meshstructure. In some embodiments, collapsing the stent portion and meshstructure includes: decoupling the inner shaft and the intermediateshaft; and advancing the inner shaft distally relative to theintermediate shaft. In some embodiments the method includes aspiratingor infusing a thrombolytic agent into or from the venous vessel before,during, or after thrombus extraction.

One aspect of the present disclosure relates to a method of treatingdeep vein thrombosis in a peripheral vasculature of a patient. Themethod includes: percutaneously accessing a venous vessel of a patientwith an introducer sheath through a popliteal access site into thevenous vessel of the patient; and inserting a catheter constraining athrombus extraction device through a lumen of the introducer sheath sothat a distal tip of the catheter is distally past a portion of thevascular thrombus in the venous vessel, which thrombus extraction deviceincludes a proximal self-expanding stent portion formed of a unitaryfenestrated structure and a distal expandable tubular portion and/orcylindrical portion formed of a braided filament mesh structure. In someembodiments, a proximal end of the mesh structure is attached to adistal end of the fenestrated structure. The method includes deployingthe thrombus extraction device from the catheter from a constrainedconfiguration to an expanded configuration by advancing an intermediateshaft distally until the stent portion of the thrombus extraction deviceis beyond a distal end of the catheter, which intermediate shaftslidably extends through the catheter and a distal end thereof iscoupled to a proximal end of the fenestrated structure. The methodincludes retracting the thrombus extraction device proximally so thatthe stent portion cores and separates a portion of the vascular thrombusfrom the venous vessel wall while the mesh structure captures thevascular thrombus portion. The method includes withdrawing the thrombusextraction device from the patient.

In some embodiments, deploying the thrombus extraction device furtherincludes retracting an inner shaft with respect to the catheter and theintermediate shaft until a stop feature on the inner shaft engages acorresponding feature on the stent portion for full expansion of thethrombus extraction device. In some embodiments, the stent portionmaintains sufficient radial force on the venous vessel wall to core andseparate the vascular thrombus portion at full expansion, and in someembodiments the inner shaft slidably extends through the intermediateshaft and a distal end thereof is coupled to a distal end of the meshstructure. In some embodiments the method includes deploying aself-expanding funnel on a distal end of the introducer sheath proximalof the vascular thrombus. In some embodiments, deploying theself-expanding funnel includes: advancing an obturator having a capturesheath feature on a distal end thereof to unsheathe the self-expandingfunnel from a constrained configuration within the capture sheathfeature to a deployed configuration free of the capture sheath feature;and removing the obturator from the introducer sheath by retracting theobturator through or outside the deployed self-expanding funnel andthrough or outside the lumen of the introducer sheath.

One aspect of the present disclosure relates to a method for removal ofthrombus from a blood vessel in a body of a patient, which blood vesselcan be an artery or a vein. The method includes: providing a thrombusextraction device including a proximal self-expanding member formed of aunitary fenestrated structure, a distal substantially cylindricalportion formed of a net-like filament mesh structure which is attachedto the unitary fenestrated structure, and an inner shaft memberconnected to a distal end of the net-like filament mesh structure;advancing a catheter constraining the thrombus extraction device througha vascular thrombus, and deploying the thrombus extraction device byeither advancing the thrombus extraction device beyond a distal end ofthe catheter or retracting the catheter relative to the thrombusextraction device, thus exposing the thrombus extraction device distallypast a portion of the thrombus and allowing expansion of the thrombusextraction device to engage a wall of the blood vessel. The methodincludes: retracting the thrombus extraction device to separate aportion of the thrombus from the vessel wall and to capture the portionof the thrombus within the net-like filament mesh structure; andwithdrawing the thrombus extraction device from the body to removethrombus from the patient.

In some embodiments, advancing the catheter includes inserting thecatheter into the blood vessel until a radiopaque distal tip of thecatheter is distally past the thrombus portion. In some embodiments, thenet-like filament mesh structure is integrally formed with thefenestrated structure so that a proximal end of the net-like filamentmesh structure is attached to a distal end of the fenestrated structure.In some embodiments, the self-expanding member of the thrombusextraction device includes a stent portion, which retracting thethrombus extraction device further includes coring the thrombus portionfrom the vessel wall with the stent portion. In some embodiments, thethrombus portion is captured with the net-like filament mesh structureby entering the net-like filament mesh structure via at least oneaperture or opening located at a proximal end of the stent portion.

In some embodiments, the thrombus extraction device is advanced beyondthe distal end of the catheter by advancing an intermediate shaftdistally through the catheter, which intermediate shaft slidably extendsthrough the catheter and a distal end of the intermediate shaft iscoupled to a proximal end of the fenestrated structure. In someembodiments the method includes, retracting the inner shaft memberrelative to the catheter and the intermediate shaft until a stop featurefixed on the inner shaft member engages a corresponding feature on thefenestrated structure and locking the inner shaft member with respect tothe intermediate shaft for full expansion of the thrombus extractiondevice. In some embodiments, the inner shaft member can be dynamicallylocked with respect to the intermediate shaft.

In some embodiments the method includes, collapsing the thrombusextraction device so as to compress the thrombus portion therein priorto withdrawing the thrombus extraction device from the body. In someembodiments, collapsing includes unlocking the inner shaft member andthe intermediate shaft and advancing the inner shaft member distallyrelative to the intermediate shaft.

In some embodiments the method includes, fluoroscopically monitoringdeployment of the thrombus extraction device and ceasing advancing thethrombus extraction device beyond the distal end of the catheter orretracting the catheter relative to the thrombus extraction device basedon a position of a first radiopaque marker located on the catheterrelative to a second radiopaque marker located on the thrombusextraction device. In some embodiments, the thrombus is located in aperipheral vasculature of the patient and the blood vessel has adiameter of at least 5 millimeters and includes at least one of afemoral vein, an iliac vein, a popliteal vein, a posterior tibial vein,an anterior tibial vein, or a peroneal vein.

In some embodiments the method includes, percutaneously accessing ablood vessel that can be venous vessel of the patient with an introducersheath through a popliteal access site and inserting the catheterthrough a lumen of the introducer sheath and into the venous vessel ofthe patient. In some embodiments the method includes, percutaneouslyaccessing a venous vessel of the patient with an introducer sheaththrough a femoral access site and inserting the catheter through a lumenof the introducer sheath and into the venous vessel of the patient,which thrombus extraction device extends within a popliteal sheath andretraction of the thrombus of the extraction device is in a direction ofblood flow. In some embodiments the method includes, percutaneouslyaccessing a venous vessel of the patient with an introducer sheaththrough an internal jugular access site and inserting the catheterthrough a lumen of the introducer sheath and into the venous vessel ofthe patient, which thrombus extraction device extends within a poplitealsheath extending from the patient and retraction of the thrombus of theextraction device is in a direction of blood flow. In some embodimentsthe method includes, aspirating or infusing a thrombolytic agent into orfrom the blood vessel before, during, or after thrombus extraction.

One aspect of the present disclosure relates to a thrombus extractiondevice for removal of a vascular thrombus from a blood vessel of apatient. The thrombus extraction device includes: a catheter having aproximal end and a distal end, an outer shaft defining a first lumen, anintermediate shaft defining a second lumen, and an inner shaft, whichintermediate shaft is coaxial the first lumen and the inner shaft iscoaxial the second lumen; a proximal self-expanding coring elementformed of a unitary fenestrated structure having a proximal end and adistal end and configured to core and separate a portion of the vascularthrombus from the blood vessel, which proximal end of the fenestratedstructure is coupled to the distal end of the intermediate shaft; and adistal expandable cylindrical portion formed of a braided filament meshstructure having a proximal end and a distal end and configured tocapture the vascular thrombus portion, which proximal end of the meshstructure is attached to the distal end of the fenestrated structure,and which distal end of the mesh structure is coupled to the distal endof the inner shaft. In some embodiments, full expansion of the meshstructure and fenestrated structure varies based on a position of theintermediate shaft relative the inner shaft of the catheter.

In some embodiments, the coring element includes a stent. In someembodiments, the stent includes a ring feature slidably coupled to theinner shaft and/or to one or several strut(s) of the stent and the innershaft includes a stop feature fixed to the inner shaft, which stopfeature is configured to engage with the ring feature when the meshstructure and the stent are in full expansion.

In some embodiments the device includes, a locking mechanism that cansecure the inner shaft relative to the intermediate shaft when the meshstructure and the stent are in full expansion. In some embodiments, thelocking mechanism can maintain a desired radial force on a vessel wallwhen the stent is compressed. In some embodiments, the locking mechanismmoveably secures the inner shaft relative to the intermediate shaft viaa spring.

In some embodiments, the proximal end of the mesh structure isintegrally formed with the distal end of the fenestrated structure tocreate a unitary structure. In some embodiments, the coring element andthe mesh structure are receivable within the outer shaft. In someembodiments, the coring element and mesh structure are in a constrainedconfiguration when received within the outer shaft and an expandedconfiguration when free of the constraining outer shaft.

In some embodiments, the mesh structure includes a plurality of radialribs or grooves longitudinally spaced between the proximal and distalends of the mesh structure. In some embodiments, the mesh structure hasa first pore size at a proximal portion and a second pore size at adistal portion, which first pore size is different from the second poresize. In some embodiments, the second pore size is greater than thefirst pore size.

In some embodiments, the proximal end of the fenestrated structure iscoupled to the distal end of the intermediate shaft via a plurality ofstruts extending at a coring angle relative to a longitudinal axis ofthe thrombus extraction device. In some embodiments, the coring angle isin a range between 30 degrees and 45 degrees. In some embodiments, thecoring element has a length in a range between 25 millimeters and 100millimeters and the mesh structure has a length in a range between 100millimeters and 500 millimeters in, for example, the collapsed state. Insome embodiments, the coring element has a diameter in a range between 8millimeters and 25 millimeters at full expansion and the mesh structurehas a diameter in a range between 8 millimeters and 25 millimeters atfull expansion.

In some embodiments, the fenestrated structure includes a plurality ofinterconnected struts. In some embodiments, the proximal end of thefenestrated structure has fewer struts than the distal end of thefenestrated structure to thereby facilitate collapse of the coringelement and to facilitate maintenance of a coring orientation when theblood vessel is tortuous. In some embodiments, the fenestrated structureincludes a plurality of interconnected struts defining an opening at theproximal end of the fenestrated structure. In some embodiments, at leastsome of the plurality of interconnected struts defining the openinginclude a sharpened proximal edge.

In some embodiments the device includes, a first radiopaque markerlocated on the outer shaft and a second radiopaque marker located on thedistal end of the inner shaft. In some embodiments the device includes,a locking mechanism that can secure a relative position of the outershaft with respect to the intermediate shaft. In some embodiments thedevice includes, a handle including a plunger that can control arelative position of the inner shaft with respect to the intermediateshaft and to selectively secure the relative position of the inner shaftwith respect to the intermediate shaft.

One aspect of the present disclosure relates to an introducer sheath foraccessing and removing thrombus within a blood vessel of a patient. Theintroducer sheath includes: an elongate sheath including a proximal end,a distal end, and a lumen extending therebetween; a self-expandingfunnel affixed to the distal end of the elongate sheath; and anobturator including an elongate shaft having a capture sheath locatedproximate to a distal end of the obturator, which capture sheath canretain the self-expanding funnel in a constrained configuration and theobturator is configured to be received within the lumen of the elongatesheath.

In some embodiments the introducer sheath includes, a sealed hub locatedat the proximal end of the elongate sheath. In some embodiments, thesealed hub includes an aspiration port. In some embodiments, theself-expanding funnel has a diameter equal to or less than a diameter ofthe elongate sheath when the self-expanding funnel is in the constrainedconfiguration. In some embodiments, the obturator includes an atraumatictip located at the distal end of the obturator, which atraumatic tip isradiopaque. In some embodiments, the obturator includes a connectionfitting configured to sealingly connect with the distal end of theelongate sheath. In some embodiments, the self-expanding funnel ispermeable to blood. In some embodiments, the self-expanding funnelincludes a conical shape formed from at least one of a castellatednitinol braid, a nitinol braided stent, a laser cut nitinol, a laser cutpolymer tube, an injection molded polymeric structure, or an inflatableballoon.

One aspect of the present disclosure relates to a method of accessingand removing thrombus from a venous vessel of a patient. The methodincludes: providing an introducer sheath including an elongate sheathdefining a lumen, a self-expanding funnel affixed to a distal end of theelongate sheath, and an elongate obturator extending through the lumenand retaining the self-expanding funnel in a constrained configurationwithin a capture sheath of the obturator; percutaneously accessing avenous vessel of a patient with the introducer sheath through an accesssite, which access site includes a popliteal access site, a femoralaccess site, or an internal jugular access site; advancing a distal endof the introducer sheath to a position proximal of a thrombus; deployingthe self-expanding funnel from the constrained configuration within thecapture sheath to an expanded configuration free of the capture sheath;capturing thrombus in the self-expanding funnel; and aspirating thecaptured material through the lumen of the elongate sheath.

In some embodiments, deploying the self-expanding funnel includesdistally advancing the obturator relative to the elongate sheath tounsheathe the self-expanding funnel from the constrained configurationto the expanded configuration and removing the obturator from theintroducer sheath by proximally retracting the obturator through thedeployed self-expanding funnel and through the lumen of the elongatesheath. In some embodiments, deploying the self-expanding funnelincludes proximally retracting the sheath over the obturator tounsheathe the self-expanding funnel from the constrained configurationto the expanded configuration and removing the obturator from theintroducer sheath by proximally retracting the obturator through oroutside of the deployed self-expanding funnel and through or outside ofthe lumen of the elongate sheath.

In some embodiments the method includes, inserting a catheterconstraining a thrombus extraction device through the lumen of theelongate sheath so that a distal tip of the catheter is distally pastthe vascular thrombus portion, deploying the thrombus extraction devicefrom the catheter, and proximally retracting the thrombus extractiondevice relative to the introducer sheath until an opening of thethrombus extraction device is within the self-expanding funnel. In someembodiments the method includes, extruding a portion of thrombuscaptured by the thrombus extraction device through the thrombusextraction device. In some embodiments, the thrombus captured by theself-expanding funnel includes the extruded portion of thrombus capturedby the thrombus extraction device.

One aspect of the present disclosure relates to a thrombectomy systemfor removal of a vascular thrombus from a blood vessel of a patient. Thethrombectomy system includes: a thrombus extraction catheter including athrombus extraction device. The thrombus extraction devices includes: aproximal self-expanding coring element formed of a unitary fenestratedstructure; and a distal expandable cylindrical portion formed of abraided filament mesh structure having a proximal end attached to adistal end of the fenestrated structure. The thrombectomy systemincludes: a catheter including a lumen constraining the thrombusextraction device, an intermediate shaft connected to a proximal end ofthe self-expanding coring element, and an inner shaft connected to adistal end of the expandable cylindrical portion and slidablydisplaceable with respect to the intermediate shaft to control expansionof the expandable cylindrical portion. The thrombectomy system includes:an introducer sheath including: an elongate sheath defining an insertionlumen; a self-expanding funnel affixed to a distal end of the elongatesheath; and an elongate obturator including a sheath capture featureconfigured to retain the self-expanding funnel in a constrainedconfiguration.

In some embodiments, the obturator is configured to be received withinthe lumen of the elongate sheath and includes a connection fittingconfigured to sealingly connect with a distal end of the elongatesheath. In some embodiments, the self-expanding funnel has a length thatis at least equal to a length of the self-expanding coring element. Insome embodiments, the introducer sheath includes a self-sealing aperturelocated at a proximal end of the introducer sheath.

In some embodiments the thrombectomy system includes, an aperturedilator sized to be receivable within the self-sealing aperture andhaving an internal diameter larger than a diameter of the self-sealingaperture in a sealed configuration. In some embodiments, the introducersheath includes an aspiration port located at a proximal end of theinserter sheath, which aspiration port is selectably fluidly connectedto the insertion lumen via an aspiration valve.

In some embodiments, the insertion lumen is sized to slidably receivethe thrombus extraction catheter. In some embodiments, the expandablecylindrical portion is formed on the self-expanding coring element toform a unitary thrombus extraction device.

One aspect of the present disclosure relates to a method ofmanufacturing a unitary thrombus extraction device including a proximalfenestrated structure including a plurality of struts and a distalnet-like filament mesh structure formed on a distal end of thefenestrated structure. The method includes: identifying a plurality offormation points formed by some of the plurality of struts of theunitary fenestrated structure; threading a unique pair of wiresincluding a first wire and a second wire overlaying the first wirethrough each of the formation points; and weaving the net-like filamentmesh structure from the unique pairs of wires such that one of: thefirst wires and the second wires do not form loops about the formationpoints through which the first wires and second wires are threaded, andsuch that the other of: the first wires and the second wires form loopsabout the formation points through which the first wires and the secondwires are threaded.

In some embodiments, the net-like filament mesh structure is woven fromthe unique pairs of wires such that the first wires do not form loopsabout the formation points through which the first wires are threadedand such that the second wires form loops about the formation pointsthrough which the second wires are threaded. In some embodiments, eachof the formation points includes a peak strut. In some embodiments, thefenestrated structure includes 12 peak struts. In some embodiments, thenet-like filament mesh includes 48 wires. In some embodiments, thenet-like filament mesh structure is manually woven. In some embodiments,the net-like filament mesh structure is automatically woven.

Further areas of applicability of the present disclosure will becomeapparent from the detailed description provided hereinafter. It shouldbe understood that the detailed description and specific examples, whileindicating various embodiments, are intended for purposes ofillustration only and are not intended to necessarily limit the scope ofthe disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view of one embodiment of a thrombectomy systemfor removal of a thrombus from a blood vessel of a patient.

FIG. 2 is a side view of one embodiment of the thrombus extractioncatheter having a thrombus extraction device is a deployedconfiguration.

FIG. 3 is a side view of one embodiment of the thrombus extractioncatheter having a thrombus extraction device is a deployed configurationat full expansion.

FIG. 4 is a side view of one embodiment of a self-expanding coringelement.

FIG. 5 is a top view of one embodiment of a self-expanding coringelement.

FIG. 6 is a front view of one embodiment of a self-expanding coringelement.

FIG. 7 is a side view of one embodiment of the thrombus extractiondevice in a full expansion configuration.

FIG. 8 is a view of one embodiment of a ball shaped thrombus captured ina thrombus extraction device.

FIG. 9 is a side view of one embodiment of the braided filament meshstructure having multiple pore sizes.

FIG. 10 is a side view of one embodiment of the thrombus extractiondevice including a plurality of circumferential grooves.

FIG. 11 is a schematic illustration of one embodiment of a weavingpattern for forming the cylindrical portion and/or the braided filamentmesh structure onto the self-expanding coring element.

FIG. 12 is a section view of an embodiment of the handle with a plungerin a first position.

FIG. 13 is a section view of an embodiment of the handle with a plungerin a second position.

FIG. 14 is a close-up, section view of a portion of the handle with aplunger in a second position.

FIG. 15 is a side view of one embodiment of an obturator having aconstant dimension of an elongate shaft.

FIG. 16 is a side view of one embodiment of an obturator having avariable dimension of an elongate shaft.

FIG. 17 is a detailed section view of one embodiment of the capturesheath of the obturator.

FIG. 18 is a side view of one embodiment of an introducer sheath in anundeployed configuration.

FIG. 19 is a side view of one embodiment of an introducer sheath in apartially deployed configuration.

FIG. 20 is a side view of one embodiment of an introducer sheath in adeployed configuration.

FIG. 21 is a side view of one embodiment of an introducer sheathcomprising an inflatable balloon.

FIG. 22 is a schematic depiction of one embodiment of accessing theblood vessel via a popliteal access site.

FIGS. 23-A through 23-H are views depicting one embodiment of a processfor fully expanding the thrombus extraction device in a blood vessel.

FIGS. 24-A and 24-B are views depicting alternative steps in the processfor fully expanding the thrombus extraction device in a blood vessel.

FIGS. 25-A through 25-H are views depicting one embodiment of a processfor removal of thrombus with an expanded thrombus extraction device.

FIG. 26 is a schematic depiction of one embodiment of accessing theblood vessel via an internal jugular access site.

FIG. 27 is a schematic depiction of one embodiment of accessing theblood vessel via a popliteal access site with an extension sheath 2300.

FIG. 28 is a schematic depiction of one embodiment of accessing theblood vessel via a popliteal access site and a femoral access site.

DETAILED DESCRIPTION OF THE INVENTION

The present disclosure relates to a thrombectomy system for removal of avascular thrombus from a blood vessel of a patient. The thrombectomysystem can remove thrombus from a blood vessel, and particularly from avenous vessel of a patient via the coring of the thrombus and/or theseparating of the thrombus from the walls of the blood vessel that canoccur when the thrombectomy system is retracted through the vascularthrombus. Thrombus that is cored and/or separated from the walls of theblood vessel can be captured within the thrombectomy system and removedfrom the patient.

The thrombectomy system can include a thrombus extraction catheterincluding a Thrombus Extraction Device (“TED”). The TED can include aproximal self-expanding coring element that can be a stent portionand/or that can be formed of a unitary fenestrated structure. The TEDcan include a distal expandable cylindrical portion formed of a braidedfilament mesh structure. The braided filament mesh structure can beformed on the coring element to thereby form a unitary TED. This formingof the braided filament mesh structure directly on the coring elementcan eliminate problems, such as: inconsistent material properties,decreased flexibility, decreased strength, and/or quality controlissues, arising from connecting the braided filament mesh structure tothe coring element via, for example, welding or adhesive.

The expansion of the TED can be controlled by the relative movement ofportions of the thrombus extraction catheter. For example, a proximalend of the TED, and specifically a proximal end of the self-expandingcoring element can be connected to an intermediate shaft that isslidable within an outer shaft of the thrombus extraction catheter. Adistal end of the TED, and specifically a distal end of the expandablecylindrical portion can be connected to an inner shaft that is slidablewithin the intermediate shaft of the thrombus extraction catheter. Asthe inner shaft and the intermediate shaft are slidable with respect tothe outer shaft, the TED can be withdrawn into the outer shaft toconstrain the TED to an undeployed configuration, also referred toherein as a constrained configuration. Similarly, the TED can bedeployed from the outer shaft by the relative movement of theintermediate shaft with respect to the outer shaft. After the TED hasbeen deployed from the outer shaft, the inner shaft and the intermediateshaft can be moved with respect to each other to either expand orcontract the expandable cylindrical portion of the TED and to bring theself-expanding coring element to full expansion.

The thrombectomy system can include an introducer sheath that can besized to slidably receive the outer sheath of the thrombus extractioncatheter. The introducer sheath can include a sealed aperture at aproximal end of the introducer sheath and a self-expanding funnel. Theself-expanding funnel can be located at a distal end of the introducersheath and can be selectably held in a constrained position by a capturesheath. In some embodiments, the self-expanding funnel can be slidablycontained within the introducer sheath and can specifically be slidablewith respect to the distal end of the introducer sheath. In someembodiments, the self-expanding funnel can be distally slide from aconstrained configuration within the introducer sheath to a deployedconfiguration at which the self-expanding funnel extends from the distalend of the capture sheath.

The self-expanding funnel can be sized to engage with the self-expandingcoring element when the TED is retracted towards the funnel. As the TEDis retracted into the funnel, the funnel compresses the TED, andspecifically the coring element, and guides the TED, and specificallythe coring element into a lumen defined by the introducer sheath. TheTED can be retracted until it is completely contained within theintroducer sheath, and then the TED and the thrombus captured in the TEDcan be removed from the patient via the sealed aperture.

The thrombectomy system can access the blood vessel containing thethrombus via a plurality of access sites. These can include, forexample, an internal jugular (IJ) access site, a femoral access site, apopliteal access site, or other venous or arterial access sites. Thethrombectomy system can be used to extract thrombus and/or embolus froma variety of venous and/or arterial vessels, which can be peripheralvessels, including any vessel, including, by way of non-limitingexample, a venous vessel, having a diameter of at least 5 millimeters(mm). The thrombectomy system can be inserted through an access pointinto a circulatory system of a patient and can be advanced to a positionproximate to the thrombus. The TED can then be advanced through thethrombus, and, after being expanded distally of the thrombus, the TEDcan be retracted through the thrombus, thereby capturing all or portionsof the thrombus.

With reference now to FIG. 1 , one embodiment of a thrombectomy system100, also referred to herein as a thrombus extraction system 100, isshown. The thrombectomy system 100 can be used to access a portion of ablood vessel such as a venous vessel containing thrombus and thethrombectomy system 100 can be used to remove all or portions of thatthrombus from the blood vessel. The thrombectomy system 100 can includean introducer sheath 102 and a thrombus extraction catheter 104.

The introducer sheath 102 comprises an elongate member 106, alsoreferred to herein as an elongate sheath 106, having a proximal end 108and a distal end 110. The elongate member 106 can be elastic and/orflexible. The elongate member 106 can comprise any desired length andany desired diameter. In some embodiments, the elongate sheath 106 canhave an outer diameter of at least 10 French, at least 12 French, atleast 14 French, at least 18 French, at least 20 French, at least 22French, between 14 French and 24 French, between 15 French and 21French, between 16 French and 22 French, and/or any other orintermediate size.

The elongate member 106 can comprise a radiopaque marker that can be,for example, part of the distal end 110 of the elongate member 106. Theelongate member 106 defines a lumen extending between the proximal end108 and the distal end 110. The lumen 1701 (shown in FIG. 17 ) of theelongate member 106 can be sized to slidably receive the thrombusextraction catheter 104. In some embodiments, the lumen 1701 of theelongate member 106 can have an internal diameter of at least 2 French,at least 10 French, at least 14 French, at least 18 French, at least 20French, at least 22 French, between 11 French and 12 French, between 10French and 22 French, between 14 French and 21 French, between 16 Frenchand 20 French, and/or any other or intermediate size. The lumen 1701 canterminate at a sealed aperture 112, also referred to herein as a sealedhub 112, located at the proximal end 108 of the elongate member 106. Insome embodiments, the sealed aperture 112 can be self-sealing and/or cancomprise a self-sealing seal.

The introducer sheath 102 can further include an aspiration port 114that can be at the proximal end 108 of the elongate member 106 and/orconnected to the proximal end 108 of the elongate member 106 via, forexample, a connecting tube 116. In some embodiments, the aspiration port114 can be a part of, and/or connected to the sealed hub 112. In someembodiments, the aspiration port 114 can be selectively fluidlyconnected to the lumen 1701 via, for example, a valve 118, also referredto herein as an aspiration valve 118, which valve 118 can be a tubingclamp that can be located at a position along the connecting tube 116between the lumen 1701 and the aspiration port 114.

The introducer sheath 102 can further hold an obturator 120, alsoreferred to herein as a dilator 120. The obturator 120 can be configuredto hold a self-expanding funnel that can be attached to the distal end110 of the elongate member 106 in a constrained configuration, and torelease the self-expanding funnel from that constrained configuration.The obturator 120 can comprise a proximal end 122, a distal end 124, andan elongate shaft 126 extending therebetween. In some embodiments, theelongate shaft 126 can have a length that is greater than a length ofthe elongate member 106 of the introducer sheath 102. The obturator 120can further define a lumen extending through the obturator 120, whichlumen can receive a guidewire. In some embodiments, the guidewire cancomprise any desired dimensions and can, in some embodiments, have adiameter of approximately 0.035 inches. The obturator 120 can be sizedand shaped so as to be able to slidably move through the lumen of theelongate member 106.

The thrombectomy system 100 can include the thrombus extraction catheter104. The thrombus extraction catheter 104 can have a proximal end 130and a distal end 132. A handle 134, also referred to herein as adeployment handle 134, can be located at the proximal end 130 of thethrombus extraction catheter 104 and can connect to a catheter portion136, also referred to herein as the catheter 136.

The catheter 136 can include an outer shaft 138, an intermediate shaft140, and an inner shaft. The outer shaft 138 can comprise a variety oflengths and sizes. In some embodiments, the outer shaft 138 can be sizedto slidably fit within the introducer sheath 102. In some embodiments,the outer shaft 138 can have a size of at least 8 French, at least 10French, at least 11 French, at least 12 French, at least 14 French, atleast 16 French, between 8 French and 14 French, between 11 French and12 French, and/or any other or intermediate size.

Each of the outer shaft 138, the intermediate shaft 140, and the innershaft can define a lumen that can be a central, axial lumen. In someembodiments, the intermediate shaft 140 can be sized and/or shaped toslidably fit within the lumen 802 (shown in FIG. 8 ) of the outer shaft138 such that the intermediate shaft 140 and the outer shaft 138 arecoaxial. Similarly, in some embodiments, the inner shaft can be sizedand/or shaped to slidably fit within the lumen 804 (shown in FIG. 8 ) ofthe intermediate shaft 140 such that the inner shaft and theintermediate shaft 140 are coaxial. In this configuration, each of theouter shaft 138, the intermediate shaft 140, and the inner shaft can bedisplaced relative to the others of the outer shaft 138, theintermediate shaft 140, and the inner shaft.

In some embodiments, each of the outer shaft 138, the intermediate shaft140, and the inner shaft can have the same length, and in someembodiments some or all of the outer shaft 138, the intermediate shaft140, and the inner shaft can have different lengths. In someembodiments, for example, the intermediate shaft 140 can be relativelylonger than the outer shaft 138, and in some embodiments, the innershaft can be relatively longer than the intermediate shaft 140.

The thrombus extraction catheter 104 can further include a thrombusextraction device (TED). The TED can connect to the intermediate shaft140 and the inner shaft, and can be contained in an undeployedconfiguration within the lumen 802 of the outer shaft 138. In someembodiments, the relative positioning of the outer shaft 138, theintermediate shaft 140, and/or the inner shaft can result in the TEDbeing in an undeployed configuration, a deployed configuration, apartial expansion configuration, and/or a full expansion configuration.In some embodiments, the TED in the deployed configuration can be ineither the full expansion configuration or in the partial expansionconfiguration.

The handle 134 can include a distal end 142, also referred to herein asa lock end 142, and a proximal end 144, also referred to herein as aplunger end 144. In some embodiments, the intermediate shaft 140connects to, and distally extends towards the distal end 132 of thethrombus extraction catheter 104 from the distal end 142 of the handle134.

As seen in FIG. 1 , the distal end 142 of the handle 134 can include alock feature 146 such as, for example, a spinlock. The lock feature 146can selectively engage and/or lockingly engage with a mating feature 148located on a proximal end 150 of the outer sheath 138. In someembodiments, for example, the outer sheath 138 can proximally slide overthe intermediate sheath 140 until the lock feature 146 engages with themating feature 148 to thereby secure the position of the outer sheath138 with respect to the intermediate sheath 140. In embodiments in whichthe intermediate shaft 146 is relatively longer than the outer shaft138, a portion of the intermediate shaft 146 distally extends from adistal end 152 of the outer shaft 138 when the outer shaft 138 islockingly engaged with the lock feature 146.

The handle 134 can include a plunger 154 that can be movable between afirst, non-extended position and a second, extended position. In someembodiments, the plunger 154 can be moved from the first position to thesecond position by proximally displacing the plunger 154 relative to thehandle 134. The plunger 154 can be lockable in one or both of the firstposition and/or the second position.

The plunger 154 can connect to the inner shaft such that the inner shaftis displaceable relative to the handle 134, the outer shaft 138, and/orthe intermediate shaft 140 via the movement of the plunger 154 from thefirst position to the second position. In some embodiments in which theinner shaft is relatively longer than the intermediate shaft 140 and/orthe outer shaft 138, the inner shaft can have a length such that theinner shaft distally extends past a distal end of the intermediate shaft140 regardless of whether the plunger 154 is in the first position orthe second position.

The thrombus extraction catheter 104 can further include a first flushport 155 connecting to the outer shaft 138 and a second flush port 156connecting to the handle 134. In some embodiments, the first flush port155 can be fluidly connected to the lumen 802 of the outer shaft 138 soas to allow the flushing of the lumen 802 of the outer shaft 138 via thefirst flush port 155. In some embodiments, the second flush port 156 canbe fluidly connected to an internal portion of the handle 134 andthereby the lumen of the intermediate shaft 140 so as to allow theflushing of the lumen of the intermediate shaft 140.

The thrombectomy system 100 can further include a loading funnel 158.The loading funnel 158 can include a funnel portion 160 and a shaftportion 162. The funnel portion 160 can define a funnel shaped interiorvolume connecting to a lumen of the shaft portion 162. The funnel shapedinterior volume can be sized and shaped to receive the self-expandingfunnel and to move the self-expanding funnel to a constrained positionas the self-expanding funnel is advanced through the funnel portion 160.The funnel shaped interior volume and the lumen can be sized to allowthe distal end 124 of the obturator 120 to pass completely through theloading funnel 158.

In some embodiments, the loading funnel 158 can be configured tofacilitate loading of the self-expanding funnel into the obturator 102.In some embodiments, the self-expanding funnel can be loaded byinserting the obturator 120 through the elongate member 106 such thatthe obturator 120 extends from the distal end 110 of the elongate member106 and beyond the self-expanding funnel. The loading funnel 158 canthen be proximally slid over the obturator 120 and the self-expandingfunnel until the self-expanding funnel is fully encapsulated by theloading funnel 158 and/or until the self-expanding funnel is in theconstrained configuration. The obturator 120 can then be retracted tothereby load and/or capture the self-expanding funnel within a portionof the obturator 120, and the loading funnel 158 can then be removedfrom the obturator 120 and the elongate member 106.

The thrombectomy system 100 can further include a sealed hub dilator170, also referred to herein as a seal dilator 170 and/or an aperturedilator 170. A section view of seal dilator 170 is shown in FIG. 1 . Theseal dilator 170 can be sized and shaped for insertion into the sealedaperture 112 prior to removal of thrombus through the sealed aperture112. By this insertion into the sealed aperture 112, the seal dilator170 can dilate the sealed aperture 112. In some embodiments, thisdilation of the sealed aperture 112 can prevent the application of forcefrom the sealed aperture 112 onto the thrombus during removal of thethrombus through the sealed aperture 112. In some embodiments, the sealdilator 170 can comprise an insertion portion 172 configured tofacilitate the insertion of the seal dilator 170 into the sealedaperture 112. The seal dilator 170 can further comprise a body portion174 that can, alone, or together with the insertion portion 172 definean extraction lumen 176 through which the thrombus can be removed fromthe lumen 1701 of the elongate member 106. In some embodiments, theinternal diameter of the extraction lumen 176 can be larger than adiameter of the sealed aperture 112 in a sealed configuration

With reference now to FIG. 2 , a side view of one embodiment of thethrombus extraction catheter 104 is shown. The thrombus extractioncatheter 104 includes the handle 134, the outer shaft 138, theintermediate shaft 140, the inner shaft 200, and the thrombus extractiondevice 202, also referred to herein as the TED 202. As shown in FIG. 2 ,the outer shaft 138 is proximately displaced relative to the handle 134such that the mating feature 148 of the outer shaft 138 is contactingthe locking feature 146 of the handle 134. Due to this positioning ofthe outer shaft 138 with respect to the handle 134, each of theintermediate shaft 140, the inner shaft 200, and the TED 202 distallyextend beyond a distal end 204 of the outer shaft 138. The thrombusextraction device 202 shown in FIG. 2 is in a deployed and partialexpansion configuration.

The thrombus extraction device 202 can include a self-expanding coringelement 206, and an expandable cylindrical portion 208. Theself-expanding coring element 206 can be relatively more proximallylocated on the thrombus extraction catheter 104 than the expandablecylindrical portion 208. The self-expanding coring element 206 caninclude a proximal end 210 connecting to a distal end 212 of theintermediate shaft 140 and a distal end 214 connecting to a proximal end216 of the expandable cylindrical portion 208. The distal end 217 of theexpandable cylindrical portion 208 can connect to a distal end 218 ofthe inner shaft 200.

In some embodiments, the distal end 218 of the inner shaft 200 canfurther include a tip 220 such as an atraumatic tip and/or a radiopaquemarker 222. In some embodiments, the tip 220 can include the radiopaquemarker 222. Further radiopaque markers can be located on, for example,the outer shaft 138 and specifically the distal end 204 of the outershaft 138 and/or the distal end 212 of the intermediate shaft 140. Insome embodiments, one or both of the distal end 204 of the outer shaft138 and the distal end 212 of the intermediate shaft 140 can eachcomprise a radiopaque marker. In some embodiments, the atraumatic tip220 can define a channel configured to allow the guidewire to passthrough the atraumatic tip 220.

With reference now to FIG. 3 , a side view of one embodiment of thethrombus extraction catheter 104 with the thrombus extraction device 202in the deployed and full expansion configuration is shown. In contrastto the embodiment of FIG. 2 , the plunger 154 is in the second position,proximally retracted from the handle 134, and the inner shaft 200 isthereby proximally retracted relative to the intermediate shaft 140 tothereby fully expand the expandable cylindrical portion 208 and twosecure the expandable cylindrical portion 208 and the self-expandingcoring element 206 in full expansion configurations and/or in fullexpansion.

The thrombus extraction catheter 104 can comprise one or severalfeatures configured to secure the thrombus extraction device 202, andspecifically the self-expanding coring element 206 and/or the expandablecylindrical portion 208 in a fully expanded position and/or in fullexpansion. As used herein, full expansion occurs when the thrombusextraction device 202 is deployed and when the plunger 154 is in thesecond position. In some embodiments, one or several dimensions of thethrombus extraction device 202 can vary when the thrombus extractiondevice 202 is in full expansion. In some embodiments, this canfacilitate apposition of the walls of the blood vessel by the thrombusextraction device 202 and/or a desired force or force level applied tothe walls of the blood vessel by the thrombus extraction device 202.

In some embodiments, the plunger 154 can be locked in the secondposition by, for example, rotating the plunger 154 with respect to thehandle 134 to thereby engage one or several locking features on theplunger 154 and in the handle 134. In some embodiments, by locking theplunger 154 in the second position, the thrombus extraction device 202,and specifically the self-expanding coring element 206 and/or theexpandable cylindrical portion 208 can be secured in the full expansionby securing the position of the inner shaft 200 with respect to theintermediate shaft 140. In some embodiments, securing the position ofthe inner shaft 200 with respect to the intermediate shaft 140 caninclude locking the inner shaft 200 with respect to the intermediateshaft 140 and/or coupling the position of the inner shaft 200 withrespect to the position of the intermediate shaft 140. In someembodiments, this locking and/or coupling can be static, referred toherein as statically locked and/or statically coupled, in that theposition of the inner shaft 200 is fixed with respect to the position ofthe intermediate shaft 140, and in some embodiments, this locking and/orcoupling can be dynamic, referred to herein as dynamically locked and/ordynamically coupled, in that the position of the inner shaft 200 withrespect to the intermediate shaft 140 is limited. In some embodiments,and as will be discussed at greater length below, the inner shaft 200can be dynamically locked to the plunger 154 via a compliance spring1214 which allows some movement of the inner shaft 200 with respect tothe intermediate shaft 140 when the plunger is locked in the secondposition. Thus, in such an embodiment, the inner shaft 200 isdynamically locked and/or dynamically coupled to the intermediate shaft140 and/or with respect to the intermediate shaft 140.

With reference now to FIG. 4 , a side view of one embodiment of theself-expanding coring element 206 is shown. The self-expanding coringelement 206 can comprise a variety of shapes and sizes and can be madefrom a variety of materials. In some embodiments, the self-expandingcoring element can be made from a shape memory material such as, forexample, a shape memory alloy and/or a shape memory polymer. In someembodiments, the self-expanding coring element 206 can comprise anitinol and/or a nitinol alloy.

The self-expanding coring element 206 can be made using a variety oftechniques including, for example, welding, laser welding, cutting,laser cutting, expanding, or the like. In some embodiments, theself-expanding coring element 206 can be laser cut from a piece ofnitinol such as, for example, a nitinol tube, after which theself-expanding coring element 206 can be blown up and/or expanded.

The self-expanding coring element 206 can comprise a unitary fenestratedstructure 400 and/or a stent or a stent portion that can be configuredto core and separate a portion of a thrombus such as a vascular thrombusfrom the blood vessel containing the thrombus. This unitary fenestratedstructure 400 can comprise a plurality of struts 402 that togetherdefine a plurality of interstices 404. The struts can comprise a varietyof shapes and sizes, and in some embodiments, the struts can have athickness and/or diameter between approximately 0.05 and 0.15 inches,between approximately 0.075 and 0.125 inches, between approximately 0.09and 0.1 inches, and/or of approximately 0.096 inches.

In some embodiments, the self-expanding coring element 206 can comprisea first region 406 and a second region 408. The second region 408 can begenerally tubular and can include a plurality of interconnected struts402. The first region 406, as seen in FIG. 5 , can comprise a reducednumber of struts 402 as compared to the second region to facilitate thecollapse of the self-expanding coring element 206 to a non-expandedconfiguration and to maintain a coring orientation when the blood vesselis tortuous. In some embodiments, the first region can further comprisetwo curved struts 410-A, 410-B twisting in opposite directions around acentral axis 412, also referred to herein as a longitudinal axis 412, ofthe self-expanding coring element 206 to define a mouth 414 of theself-expanding coring element 206.

In some embodiments, the connection of the self-expanding coring element206 to the intermediate shaft 140 via the two curved struts 410-A, 410-Bcan improve the operation of the thrombus extraction device 202 byflexibly connecting the self-expanding coring element 206 to theintermediate shaft 140. Particularly, the removal of struts from region420 of the self-expanding coring element 206 allows the self-expandingcoring element 206 to flex about a connection member 415 located at theproximal end 210 of the self-expanding coring element 206 and connectingthe self-expanding coring element 206 to the intermediate shaft 140 ofthe thrombus extraction catheter 104. This ability to flex canfacilitate the maintenance of the coring orientation with the bloodvessel is tortuous. In some embodiments, such flexing of theself-expanding coring element 206 can result in the region 420functioning as the mouth 414.

As seen in FIG. 4 , the curved struts 410 extend at an angle θ, alsoreferred to herein as a coring angle, relative to the central axis 412from a bottom 416 of the self-expanding coring element 206 towards thetop 418 of the self-expanding coring element 206. In some embodiments,this angle can be between 20 degrees and 50 degrees and/or between 30degrees and 45 degrees when fully expanded.

In some embodiments, the coring angle can either positively or adverselyaffect the operation of the TED 202. For example, too steep a coringangle can prevent the self-expanding coring element 206 from beingcollapsible and thus prevent the retraction of the self-expanding coringelement 206 into the introducer sheath 102. Additionally, too shallow acoring angle can result in the self-expanding coring element 206 tooeasily collapsing which can decrease the coring ability of theself-expanding coring element 206. In some embodiments, this decrease inthe coring ability of the self-expanding coring element 206 can resultin the self-expanding coring element 206 no longer effectively coringthrombus.

In some embodiments, the most proximal edge of the two curved struts410-A, 410-B, referred to herein as a leading edge 411, can be sharpenedand/or the leading edge 411 of the two curved struts 410-A, 410-B cancomprise a cutting element, knife, or the like

The self-expanding coring element 206 can comprise a variety of sizes.In some embodiments, the self-expanding coring element 206 can comprisea length, defined as the shortest distance between the proximal end 210of the self-expanding coring element 206 and the distal end 214 of theself-expanding coring element 206, of between approximately one and 3inches, between approximately 1.5 and 2.5 inches, between approximately1.75 and 2.25 inches, between approximately 1.9 2.0 inches, and/or ofapproximately 1.96 inches. In some embodiments, the self-expandingcoring element 206 can comprise a fully expanded diameter betweenapproximately 2 and 50 mm, between approximately 4 and 25 mm, betweenapproximately 6 and 20 mm, and/or between approximately 8 and 16 mm. Insome embodiments, the self-expanding coring element can be applied todebulking of an artery or vein such as, for example, the inferior venacava. In some embodiments, such debulking can be performed in responseto the occluding and/or partial occluding of one or several filters inthe inferior vena cava.

In some embodiments, the length and the diameter of the self-expandingcoring element 206 can be selected based on the size of the bloodvessel, and particularly the diameter of the blood vessel from whichthrombus is to be extracted. In some embodiments, the length of theself-expanding coring element 206 can be selected based on the fullyexpanded diameter of the self-expanding coring element 206 to preventundesired tipping and/or rotation of the self-expanding coring elementwithin the blood vessel and with respect to the blood vessel. As usedanywhere herein, “approximately” refers to a range of +/- 10% of thevalue and/or range of values for which “approximately” is used.

With reference now to FIG. 7 , a side view of one embodiment of thethrombus extraction device 202 is shown. As seen in FIG. 7 , theself-expanding coring element 206 is connected via the connection member415 at the proximal end 210 of the self-expanding coring element 206 tothe distal end 212 of the intermediate shaft 140. The proximal end 216of the expandable cylindrical portion 208 connects to the distal end 214of the self-expanding coring element 206. In some embodiments, theexpandable cylindrical portion 208 and specifically the proximal end 216of the expandable cylindrical portion 208 is formed on the distal end214 of the self-expanding coring element 206 to thereby form a unitarythrombus extraction device 202. The distal end 217 of the expandingcylindrical portion 208 connects to the distal end 218 of the innershaft 200.

In some embodiments, and as seen in FIG. 7 , the self-expanding coringelement 206 can engage with all or portions of the inner shaft 200 toaffect the expansion of the self-expanding coring element 206.Specifically, in some embodiments, the self-expanding coring element 206can include a ring 700, also referred to herein as a ring feature 700.The ring 700 can be the same material as the self-expanding coringelement 206 or can be a different material than the self-expandingcoring element 206. The ring 700 can be integrally formed with theself-expanding coring element 206 and/or can be attached to theself-expanding coring element via, for example, one or several welds,adhesive, one or several mechanical fasteners, or the like. The ring 700can have a diameter larger than the diameter of the inner shaft 200 suchthat the ring 700 is slidable along the inner shaft 200.

As further seen in FIG. 7 , the inner shaft 200 can include a stop 702.In some embodiments, the stop 702 can comprise a polymeric member and/ormetallic member that is affixed to a portion of the inner shaft 200. Insome embodiments, the stop 702 can be sized and shaped to engage withthe ring 700 to thereby apply proximally directed force to theself-expanding coring element 206 when the inner shaft 200 is proximallydisplaced via movement of the plunger 154 to the second position. Insome embodiments, a portion of the self-expanding coring element 206located between the ring 700 and the connection member 415 can beforcibly expanded by the application of this proximally directed forceto ring 700, thereby moving the self-expanding coring member 206 to fullexpansion.

In some embodiments, the inner shaft 200 of the thrombus extractioncatheter 104 can be selectively connected to the distal end 217 of theexpandable cylindrical portion 208. This can allow the displacement ofthe inner shaft 200 to bring the self-expanding coring element 206 tofull expansion via the engagement of the ring feature 700 with the stop702. In some embodiments, and after the self-expanding coring element206 is at full expansion, the inner shaft 200 can be recoupled to thedistal end 217 of the expandable cylindrical portion 208 such that theexpandable cylindrical portion 208 is fully expanded and/or can berecoupled to the distal end 217 of the expandable cylindrical portion208 such that the expandable cylindrical portion 208 to compress theexpandable cylindrical portion 208 when the plunger 154 is moved fromthe second position to the first position.

In some embodiments, the expandable cylindrical portion 208 can comprisea braided filament mesh structure 704 that can be configured to capturethrombus. In some embodiments, the braided filament mesh structure canbe coextensive with the expandable cylindrical portion 208 and thus canshare a proximal end 216 and/or a distal end 217. In the embodimentshown in FIG. 7 , the braided filament mesh structure 704 is a braid ofelastic filaments having a generally tubular, elongated portion 706 anda distal tapered portion 708. In other embodiments, the braided filamentmesh structure 704 can be any porous structure and/or can have othersuitable shapes, sizes, and configurations (e.g., the distal portion 708can be generally cylindrical, etc.).

Due to the connection of the braided filament mesh structure 704 to thedistal end 218 of the inner shaft 200, axial movement of the inner shaft200 radially expands/shortens and collapses/lengthens the braidedfilament mesh structure 704 of the TED 200. For example, so long as theintermediate shaft 140 is fixed and/or limited to axial movement at arate less than that of the inner shaft 200: (1) distal movement of theinner shaft 200 stretches the braided filament mesh structure 704 alongits longitudinal axis such that the radius of the braided filament meshstructure 704 decreases and the length of the braided filament meshstructure 704 increases; and (2) proximal movement of the inner shaft200 compresses the braided filament mesh structure 704 along itslongitudinal axis such that the radius of the braided filament meshstructure 704 increases and the length of the braided filament meshstructure 704 decreases. In certain embodiments, the braided filamentmesh structure 704 can have a length in the collapsed configurationbetween approximately 5 and 30 inches, between approximately 10 and 20inches, and/or of approximately 16 inches, and in some embodiments, thebraided filament mesh structure 704 can have a length in the expandedconfiguration of between approximately 1 and 25 inches, betweenapproximately 10 and 20 inches, and/or of approximately 11 inches.

In some embodiments, the braided filament mesh structure 704 can beformed by a braiding machine and/or weaving machine, and in someembodiments, the braided filament mesh structure 704 can be manuallybraided and/or woven. In some embodiments, the braided filament meshstructure 704 may be formed as a tubular braid, which tubular braid maythen be further shaped using a heat setting process. In someembodiments, the braid may be a tubular braid of fine metal wires suchas nitinol (nickel-titanium alloy), platinum, cobalt-chrome alloy,stainless steel, tungsten or titanium. In some embodiments, the braidedfilament mesh structure 704 can be formed at least in part from acylindrical braid of elastic filaments. Thus, the braid may be radiallyconstrained without plastic deformation and will self-expand on releaseof the radial constraint. Such a braid of elastic filaments is hereinreferred to as a “self-expanding braid.”

In some embodiments, the thickness of the braid filaments can be lessthat about 0.15 mm. In some embodiments, the braid may be fabricatedfrom filaments and/or wires with diameters ranging from about 0.05 mm toabout 0.25 mm. In some embodiments, braid filaments of differentdiameters may be combined to impart different characteristics including:stiffness, elasticity, structure, radial force, pore size, emboliccapturing or filtering ability, etc. In some embodiments, the braidedfilament count is between 20 and 80, is greater than 30, and/or isapproximately 24. Pore sizes of the braided mesh in the elongatedportion 706 may be in the range of about 0.4 mm to 4.0 mm. In someembodiments, the pore size may be in the range of 0.5 mm to 2.5 mm.

In some cases thrombus may form a shape that is difficult to retractinto the introducer sheath 102 when thrombus is within the braidedfilament mesh structure 704. Such a case is depicted in FIG. 8 in whichthe thrombus extraction device 202, and specifically the braidedfilament mesh structure 704, is partially retracted into the introducersheath 102. As depicted in FIG. 8 , thrombus 800 has formed a ball thathas a diameter larger than the diameter of the introducer sheath 102.Such behavior by the thrombus 800 can prevent the removal of the TED 200and the thrombus 800 from the patient’s body. FIGS. 9 and 10 addressfeatures to prevent such behavior by the thrombus.

FIG. 8 further shows a cross-section view of the elongate member 106such that the lumen 1702 of the elongate member is visible, across-section of the outer shaft 138 such that the lumen 802 of theouter shaft 138 is visible, and a cross-section of the intermediateshaft 140 such that the lumen 804 of the intermediate shaft 140 isvisible.

With reference now to FIG. 9 , a side view of one embodiment of thebraided filament mesh structure 704 comprising multiple pore sizes isshown. As seen, the braided filament mesh structure 704 comprises afirst portion 900 comprising a first plurality of pores 904 and a secondportion 902 comprising a second plurality of pores 906. In someembodiments, the first portion 900 can correspond to the elongatedportion 706, and the second portion 902 can correspond to the distaltapered portion 708.

As shown in FIG. 9 , the first portion 900 of the braided filament meshstructure 704 is relatively more proximal than the second portion 902.As further shown, the pores in the first plurality of pores 904 of thefirst portion 900 are smaller than the pores in the second plurality ofpores 906 of the second portion 902. In some embodiments, the largerpores of the distal, second portion 902 can have an average size greaterthan or equal to 1.5 mm, and in some embodiments, between approximately1.0 mm and 4.0 mm.

In such an embodiment, the larger size of the pores of the secondplurality of pores 906 can allow and/or facilitate the extrusion ofportions of the thrombus when the braided filament mesh structure 704 ismoved to the unexpanded configuration and/or when the braided filamentmesh structure 704 is retracted into the introducer sheath 102. In someembodiments, this extrusion of portions of the thrombus can prevent thecase in which the thrombus cannot be retracted into the introducersheath 102. Further, in some embodiments, relatively newer portions ofthrombus can be extruded before relatively older portions of thrombus asrelatively newer portions of thrombus can be softer and/or moremalleable. These relatively newer portions of the thrombus can then becaptured and/or broken down by features of the introducer sheath 102.

With reference now to FIG. 10 , a side view of one embodiment of the TED200 comprising a plurality of circumferential depressions 1000, alsoreferred to herein as circumferential grooves, radial ribs, and/orradial grooves, is shown. In some embodiments, some or all of thisplurality of circumferential depressions 1000 can inwardly extendtowards a central axis 1002 and/or midline 1002 of the thrombusextraction device 202. In some embodiments, the plurality ofcircumferential depressions 1000 can be longitudinally spaced and/orequally spaced along the length of the expandable cylindrical portion208 and/or the braided filament mesh structure 704 between the proximalend 216 and the distal end 217 of the cylindrical portion 208 and/or thebraided filament mesh structure 704. In some embodiments, thesecircumferential depressions 1000 can, when the thrombus extractiondevice 202 is moved from an expanded configuration to an unexpandedconfiguration, engage with portions of the thrombus contained within thecylindrical portion 208 and/or the braided filament mesh structure 704to inhibit movement of the thrombus with respect to one or both of theproximal end 216 and the distal end 217 of the cylindrical portion 208and/or the braided filament mesh structure 704. This inhibition ofthrombus movement can decrease the likelihood of the creation ofthrombus that cannot be retracted into the introducer sheath 102.

Although depicted in separate figures, some embodiments of the thrombusextraction device 202 can include both the plurality of circumferentialdepressions discussed with respect to FIG. 10 and multiple pore sizes asdiscussed with respect to FIG. 9 .

With reference now to FIG. 11 , a schematic illustration of oneembodiment of a weaving pattern for forming the cylindrical portion 208and/or the braided filament mesh structure 704 onto the self-expandingcoring element 206 at one or several formation points 1103 is shown. Asseen, the self-expanding coring element 206 comprises a plurality ofstruts 402 that connect at formation points 1103 comprising peaks 1100,also referred to herein as peak struts 1100. As seen, each of the peaks1100 is formed by the intersection of a first strut 402-A and a secondstrut 402-B, which intersecting struts 402-A, 402-B form a peak aperture1101.

In some embodiments, the self-expanding coring element 206 can comprisea plurality of peaks 1100 extending around the distal end of theself-expanding coring element 206. The plurality of peaks 1100 cancomprise 4 peaks 1100, 6 peaks 1100, 8 peaks 1100, 10 peaks 1100, 12peaks 1100, 16 peaks 1100, 20 peaks 1100, 24 peaks 1100, between 4 and50 peaks, between 8 and 20 peaks, and/or any other or intermediatenumber of peaks.

The cylindrical portion 208 and/or the braided filament mesh structure704 can comprise a plurality of filaments 1102 woven and/or braidedtogether to form the cylindrical portion 208 and/or the braided filamentmesh structure 704. In some embodiments, the plurality of filaments caninclude, for each of the peaks 1100 of the self-expanding coring element206, a first filament 1104 and the second filament 1106. The first andsecond filaments 1104, 1106 can be woven onto their respective peak. Insome embodiments, the first and second filaments 1104, 1106 can be wovenonto their respective peak such that one or both of the first and secondfilaments 1104, 1106 form a loop about their respective peak. Thus, insome embodiments, the only the first filament 1104 forms a look aboutits peak, only the second filament 1106 forms a loop about its peak, orboth the first and second filaments 1104, 1106 form loops about theirpeak. With reference to the embodiment of FIG. 11 , the first filament1104 can be inserted straight through the peak aperture 1101 of its peaksuch that the first filament 1104 does not loop on itself directlyadjacent to its peak, and more specifically, directly distal of itspeak.

The first filament 1104 can be inserted through the peak aperture 1101of its peak 1100 such that the first filament 1104 passes, when lookingfrom the outside of the self-expanding coring element 206 towards theinside of the self-expanding coring element 206, on top of the firststrut 402-A and under the second strut 402-B.

The second filament 1106 can be inserted through the peak aperture 1101of its peak such that the portion of the second filament 1106 passingthrough the peak aperture 1101 is separated from the peak by the firstfilament 1104. Further, the second filament 1106 can be inserted throughthe peak aperture 1101 such that the second filament 1106 passesunderneath the first strut 402-A and over the second strut 402-B. afterinsertion through the peak aperture 1101, the second filament 1106 canbe looped on itself to form a loop 1108 directly distal to its peak 100.

In some embodiments, because each filament 1104, 1106 is insertedthrough a peak aperture 1101, each filament 1104, 1106 can be treated,for braiding or weaving purposes as comprising a first wire extendingfrom its peak 1100 to a first end of the filament 1104, 1106 and asecond wire extending from its peak to a second end of that filament1104, 1106. Thus, in some embodiments in which the self-expanding coringportion 206 comprises 12 peaks, the cylindrical portion 208 and/or thebraided filament mesh structure 704 can be formed from 24 filaments1104, 1106 which can be woven and/or braided as 48 wires to form a 48wire mesh and/or weave.

In some embodiments, the cylindrical portion 208 and/or the braidedfilament mesh structure 704 can be braided/woven by, identifying theplurality of formation points 1103 formed by some of the struts 402 ofthe self-expanding coring element 206. Unique pairs of wires can bethreaded through each of the formation points 1103, and specificallythrough the peak aperture 1101 adjacent to each of the formation points1103. In some embodiments, each unique pair of wires can comprise afirst wire 1104 and a second wire 1106 overlaying the first wire 1104.The first and second wires can then be woven into a net-like filamentmesh structure of the cylindrical portion 208 and/or the braidedfilament mesh structure 704 from the unique pairs of wires such that thefirst wires 1104 do not form loops about the formation points 1103through which the first wires 1104 are threaded and such that the secondwires 1106 form loops 1108 about the formation points 1103 through whichthe second wires 1106 are threaded.

With reference now to FIG. 12 , a section view of an embodiment of thehandle 134 in which the plunger 154 is in the first position is shown,and with reference to FIG. 13 a section view of an embodiment of thehandle 134 in which the plunger 154 is in the second position is shown.The handle 134 can include a housing 1200 that defines an internalvolume 1202. A plunger shaft 1204 can extend through all or portions ofthe internal volume 1202 and can connect to the inner shaft 200, whichinner shaft 200 can define the previously referenced lumen 1400, alsoreferred to herein as inner shaft lumen 1400. The plunger shaft 1204 canterminate at a plunger guide 1208 that is affixed to the plunger shaft1204. In some embodiments, and as seen in FIGS. 12 and 13 , the plunger154 can be biased towards a first position by a plunger spring 1209which can engage a portion of the handle 134 and the plunger guide 1208.Thus, the plunger spring 1209 is less compressed when the plunger 154 isin the first position as is shown in FIG. 12 , and the plunger spring1209 is more compressed when the plunger 154 is in the second positionas is shown in FIG. 13 . In some embodiments, this bias towards thefirst position can create a bias in the thrombus extraction device 202towards the partial expansion configuration.

As seen in FIG. 14 , a close-up view of the encircled portion “A”indicated in FIG. 13 , the plunger guide 1208 can be positioned betweena proximal stop 1210 and a distal stop 1212, which proximal stop 1210and which distal stop 1212 can be each affixed to the inner shaft 200including the inner shaft lumen 1400. The plunger guide 1208 can bedynamically connected to the proximal stop 1210 via a stent compliancespring 1214, also referred to herein as a compliance spring 1214. Insome embodiments, the use of the compliance spring 1214 to connect theplunger guide 1208 and the proximal stop 1210 can allow a change in thediameter of the self-expanding coring element 206 according tocompressive forces applied to the self-expanding coring element 206.

In some embodiments, for example, via the interaction of the ringfeature 700 and the stop 702, radial compressive forces applied to theself-expanding coring element 206 can be transferred from theself-expanding coring element 206 via the ring feature 700 and the stop702 to the compliance spring 1214. In embodiments in which thecompressive force is greater than the spring force, the compliancespring 1214 can be compressed and the inner shaft 200 can distallyadvance relative to the intermediate shaft 140 to thereby reduce thediameter of the self-expanding coring element 206 until the compressiveforce is equal to the spring force. This compliance achieved via thecompliance spring 1214 enables use of the thrombus extraction catheter104 in blood vessels that can be arteries or venous vessels ofnon-constant diameter while maintaining desired contact of theself-expanding coring element 206 on the walls of the blood vessels,veins, or venous vessels. In some embodiments, this compliance canresult in a constant outward force applied to the vessel walls by theself-expanding coring element 206 when the vessel has a diameter betweenapproximately 1 and 30 mm, 2 and 25 mm, 5 and 20 mm and/or any other orintermediate diameter. In some embodiments, this constant outward forcecan be constant in that this outward force is within a predeterminedrange. In some embodiments, for example, the outward force can beapproximately 5 N when the diameter of the self-expanding coring element206 is approximately 20 mm and the outward force can be approximately 20N when the diameter of the self-expanding coring element 206 isapproximately 5 mm. Thus, in some embodiments, a locking mechanism whichcan include the plunger 154 and the compliance spring 1214 can beconfigured to maintain a desired radial force on a vessel wall when thestent is compressed by that vessel wall. In some embodiments, thisdesired force can be a sufficient radial force on the vessel wall tocore and/or separate all or portions of thrombus from the vessel wallwhen the self-expanding coring element 206 is at full expansion.

With reference now to FIGS. 15 and 16 , side views of embodiments of theobturator 120 are shown. As seen, the obturator 120 includes theproximal end 122, the distal end 124, and the elongate shaft 126. Asfurther seen, the obturator 120 can include a capture sheath 1500proximally extending form the distal end 124 of the obturator 120.

The Obturator 120 can further comprise a tip such as an atraumatic tip1502 located at the distal end 124 of the obturator 120. In someembodiments, the atraumatic tip 1502 can be radiopaque. The obturator120 can further include a connection fitting 1504 that can be located ata proximal end 1506 of the capture sheath 1500. In some embodiments, theconnection fitting 1504 can be configured to sealingly connect with thedistal end 110 of the elongate sheath 106 of the introducer sheath 102.

The obturator 120 can further include a stop portion 1508 located at theproximal end 122 of the obturator 120. In some embodiments, the stopportion 1508 can have a diameter larger than the lumen 1701 of theelongate member 106 of the introducer sheath 102 and/or larger than thediameter of the sealed aperture 112 located at the proximal end 108 ofthe introducer sheath 102 so as to prevent the stop portion 1508 fromentering into the lumen 1701 of the elongate member 106 and/or thesealed aperture 112.

In some embodiments, the elongate shaft 126 can comprise a constant sizeand/or diameter, and in some embodiments, the elongate shaft 126 cancomprise multiple sizes and/or diameters. For example, the diameter 1510of the elongate shaft 126 shown in FIG. 15 is constant along the lengthof the elongate shaft 126. In contrast, the elongate shaft 126 shown inFIG. 16 has at least a first diameter 1512 along one or several firstportions 1513 of the elongate shaft 126 and a second diameter 1514 alongone or several second portions 1515 of the elongate shaft 126.

In some embodiments, the one or several second portions 1515 of theelongate shaft can be located along the length of the elongate shaft 126such, that when the obturator 120 is received within the elongate member106 of the introducer sheath 102 and positioned so that the connectionfitting 1504 seals with the distal end 110 of the elongate sheath 106,the one or several second portions 1515 extend through the sealedaperture 112. In such an embodiment, the second diameter 1514 can beselected such that the one or several second portions do not contactand/or dilate the sealed aperture 112 and/or a seal within the sealedaperture 112. Because such an embodiment of the obturator 120 does notdilate the seal of the sealed aperture 112 when the one or severalsecond portions extend through the sealed aperture 112, the introducersheath 102 can be stored, package, and/or sold with such an obturator120 pre-positioned extending through the lumen 1701 of the elongatemember 106.

With reference now to FIG. 17 , a detailed section view of oneembodiment of the capture sheath 1500 is shown. As seen, the capturesheath 1500 includes the atraumatic tip 1502 and is connected to theelongate shaft 126 of the obturator 120, which elongate shaft 126extends through a lumen 1701 of the elongate member 106. As furtherseen, a lumen 1700 extends through the atraumatic tip 1502 and theelongate shaft 126, which lumen 1700 can be configured to receive aguidewire.

That capture sheath 1500 includes a capture shell 1702 that distallyextends from the atraumatic tip 1502 to the proximal end 1506 of thecapture sheath 1500. The capture shell 1702 terminates in the connectionfitting 1504. The capture shell 1702 has an internal diameter 1704 thatis greater than a diameter 1706 of the portion of the elongate shaft 126extending through the capture shell 1702. Due to the larger internaldiameter 1704 of the capture shell 1500, a receiving space is createdbetween the capture shell 1702 and the portion of the elongate shaft 126extending through the capture shell 1702. In some embodiments, thisreceiving space can be sized and shaped to receive and/or retain aself-expanding funnel 1708 in a constrained configuration. In someembodiments, the self-expanding funnel 1708 can have a diameter matchingthe internal diameter 1704 of the capture shell 1702 when theself-expanding funnel 1708 is in the constrained configuration. In someembodiments, this diameter of the self-expanding funnel can be less thanor equal to a diameter 1716 of the elongate member 106.

The self-expanding funnel 1708 can comprise a variety of shapes andsizes and can be made from a variety of materials. In some embodiments,the self-expanding funnel 1708 can have a maximum diameter greater thanand/or equal to the diameter of the self-expanded coring element 206 infull expansion, and in some embodiments, the self-expanding funnel 1708can have a minimum diameter equal to the diameter 1716 of the elongatemember 106 and/or to the diameter of the lumen 1701 of the elongatemember 106. In some embodiments, the self-expanding funnel 1708 can havea length greater than and/or equal to the length of the self-expandingcoring element 206 such that the self-expanding coring element 206 canbe received and contained within the self-expanding funnel 1708.

In some embodiments, the self-expanding funnel 1708 can have a conicallyshaped portion, and specifically, a truncated-conically shaped portion.In some embodiments, the self-expanding funnel can be formed from atleast one of a castellated nitinol braid, a nitinol braided stent, alaser cut nitinol, a laser cut polymer tube, an injection moldedpolymeric structure, or an inflatable balloon. In some embodiments, theself-expanding funnel 1708 can comprise a mesh having a pore sizesufficiently small to prevent the passage of dangerous thrombus throughthe pores of the mesh. In some embodiments, the self-expanding funnel1708 can be permeable to blood.

With reference now to FIGS. 18 through 20 , side views of embodiments ofthe introducer sheath 102 in different configurations are shown. In FIG.18 the introducer sheath 102 is shown in an undeployed configuration, inFIG. 19 , the introducer sheath 102 is shown in a partially deployedconfiguration, and in FIG. 20 , the introducer sheath 102 is shown in afully deployed and/or deployed configuration.

Specifically, as seen in FIG. 18 , the obturator 120 extends through thelumen 1701 of the elongate member 106 and the self-expanding funnel 1708is contained in a constrained configuration within the capture sheath1500. In FIG. 19 , the obturator 120 has been distally advanced tothereby release the self-expanding funnel 1708 from the constrainedconfiguration and/or to deploy the self-expanding funnel 1708. In someembodiments, the length of the obturator 120, and specifically thelength of the elongate shaft between the proximal end of the capturesheath 1500 and the stop portion 1508 is sufficient to allow thedeployment of the self-expanding funnel 1708 from the capture sheath1500 before further distal movement of the obturator 120 is prevented bythe collision of the stop portion 1508 with the sealed aperture 112.

After the self-expanding funnel 1708 has been deployed, the obturator120 can be proximally retracted through the lumen 1701 of the elongatemember 106 and the sealed aperture 112 and can be removed from theintroducer sheath 102. After the obturator 120 has been removed from theintroducer sheath 102, the introducer sheath is in the fully deployedconfiguration as shown in FIG. 20 .

In some embodiments, and as seen in FIG. 21 , the introducer sheath 102can include an inflatable balloon 2100 located at, or proximate to thedistal end 110 of the elongate member 106. In some embodiments, theballoon 2100 can comprise a conically shaped internal portion 2102 thatcan be sized and shaped to receive the thrombus extraction device 202,and specifically that can have a length greater than or equal to thelength of the self-expanding coring element 206.

With reference now to FIG. 22 , an introduction technique for accessingthe thrombus 2200 is shown. As depicted, the thrombus 2200 can belocated in a blood vessel and accessed through an access site 2260 suchas the popliteal access site. The introducer sheath 102 can extend fromthe popliteal access site 2260 to the deployment position 2262 at whichthe self-expanding funnel 1708 can be deployed and which can beproximate to the thrombus 2200. The TED 202 can be passed through theclot 2200 in the direction of blood flow and the TED 202 can beretracted through the clot 2200 in a direction opposite blood flow. Theretraction of the TED 202 through the clot 2200 can result in the coringof the clot with the self-expanding coring element 206 and the capturingof the clot in the expandable cylindrical 208.

In some such embodiments, all or portions of the TED 202 can extend intoone of the iliac veins and/or the inferior vena cava as depicted in FIG.23 . Further, as the TED 202 is retracted from a proximal position withrespect to the heart to a distal position with respect to the heart, thediameter of the blood vessel 2202 will decrease as the TED 202 isretracted towards the access site 2260. This can result in increasedcompressive forces on the TED 202, and specifically on theself-expanding coring element 206. These compressive forces can betransferred via the ring feature 700 and the stop 702 to the compliancespring 1214. Via the stretching or compressing of the compliance spring1214, the diameter of the TED 202 and specifically of the coring element206 can change to match the diameter of the blood vessel and a desiredradial force, and/or force level can be maintained.

FIGS. 23-A to 23-H, FIGS. 24-A and 24-B, and FIGS. 25-A to 25-H depictprocesses for using the thrombus extraction system 100 to removethrombus from a patient’s body, and specifically from a blood vessel,which can be a venous vessel, in the patient’s body. This includes:accessing the blood vessel via one or several percutaneous access sitesthat can provide direct access to the blood vessel or indirect access tothe blood vessel via one or several other blood vessels; advancing theintroducer sheath to a position proximate to the thrombus; deploying theself-expanding funnel of the introducer sheath; advancing the distal end132 of the thrombus extraction catheter 104 to a position proximate tothe thrombus; deploying the thrombus extraction device 202; capturingthe thrombus in the thrombus extraction device 202 by retracting thethrombus extraction device 202 through the thrombus; collapsing thethrombus extraction device 202; and removing the thrombus extractiondevice 202 and the captured thrombus from the introducer sheath 102 andfrom the patient’s body. In some embodiments, these one or severalaccess sites can include, for example, a popliteal access site, afemoral access site, and/or an internal jugular access site. In someembodiments, a thrombolytic agent can be infused and/or aspirated intoor from the blood vessel before, during, or after the removal orextraction of the thrombus

The process for using the thrombus extraction system 100 shown in FIGS.22-A to 22-H, FIGS. 24-A and 24-B, and FIGS. 25-A to 25-H can beperformed with the direction of blood flow or against the direction ofblood flow. Thus, in some embodiments, the direction of blood flow inFIGS. 22-A to 22-H, FIGS. 24-A and 24-B, and FIGS. 25-A to 25-H, can befrom left to right, or from right to left.

With reference now to FIGS. 23-A to 23-H, a process for expanding thethrombus extraction device 202 in a blood vessel such as a venous vesselis shown. The process for expanding the thrombus extraction device 202in the vessel can be performed using all or portions of the thrombusextraction system 100. In some embodiments, the process for expandingthe thrombus extraction device 202 in the vessel can be performed inconnection with a monitoring technique, such as fluoroscopy,angiography, and/or ultrasonic monitoring. In some embodiments, themonitoring technique can be used to monitor the deployment of the TED202 in the vessel via observation of the one or several radiopaquemarkers located on the introducer sheath 102 and/or the thrombusextraction catheter 104.

The process begins at FIG. 23-A, wherein a thrombus 2200 is identifiedin a blood vessel 2202 such as venous vessel. In some embodiments, thethrombus 2200 can be located in the peripheral vasculature of thepatient’s body. The thrombus 2200, also referred to herein as a clot2200, can comprise a proximal end 2204 and the distal end 2206. In someembodiments, the identification of the blood vessel 2202 can furtherinclude the determination of whether the thrombus 2200 in the bloodvessel 2202 is suitable for thrombus extraction. In some embodiments,the thrombus 2200 in the blood vessel 2202 can be suitable forextraction when the blood vessel 2202 has a diameter of at least 5millimeters. In some embodiments, the thrombus 2200 in the blood vessel2202 can be suitable for extraction when the blood vessel 2202 has adiameter of at least 5 millimeters and is at least one of a femoralvein, an iliac vein, a popliteal vein, a posterior tibial vein, ananterior tibial vein, or a peroneal vein.

After the thrombus has been identified, the process proceeds to the stepshown in FIG. 23-B, wherein the introducer sheath 102 is advanced,either with or against the direction of blood flow in the blood vessel,such that the distal end 110 of the introducer sheath 102 and/or theobturator 120 is proximate to the thrombus 2200, and particularly isproximate to the thrombus 2200 at a position proximal of the thrombus2200. In some embodiments, this can include providing the introducersheath 102 and percutaneously accessing the circulatory system of thepatient and specifically a blood vessel or venous vessel of the patientvia an access site 2208 which can be one of the above referenced accesssites.

After the introducer sheath 102 has been advanced to a desired position,the self-expanding funnel 1708 can be deployed and/or unsheathed fromthe constrained configuration to the expanded configuration as depictedin FIG. 23-C. In some embodiments, the self-expanding funnel 1708 can bedeployed by the relative distal movement of the obturator 120 withrespect to the elongate member 106 until the funnel 1708 is no longerconstrained by the capture sheath 1500 and then the obturator 120 can beproximally retracted through the lumen 1701 of the elongate member 106until the obturator 120 is removed from the introducer sheath 102.

In some embodiments, the relative distal movement of the obturator 120with respect to the elongate member can comprise fixing the position ofthe obturator 120 relative to the blood vessel 2202 and proximallyretracting the elongate member 106 over the obturator 120 to unsheathethe self-expanding funnel 1708 until the stop 1508 contacts the sealedaperture 112 and/or until monitoring, which can be fluoroscopicmonitoring, of radiopaque markers located in, for example, the tip 1502of the obturator 120 and the distal end 110 of the elongate member 106indicate that the self-expanding funnel 1708 is deployed and/or is nolonger constrained by the capture sheath 1500. Alternatively, in someembodiments, the relative distal movement of the obturator 120 withrespect to the elongate member can comprise fixing the position of theelongate member 106 relative to the blood vessel 2202 and distallyadvancing the obturator 120 two unsheathe the self-expanding funnel 1708until the stop 1508 contacts the sealed aperture 112 and/or untilmonitoring, which can be fluoroscopic monitoring, of radiopaque markerslocated in, for example, the tip 1502 of the obturator 120 and thedistal end 110 of the elongate member 106 indicate that theself-expanding funnel 1708 is deployed and/or is no longer constrainedby the capture sheath 1500.

After the self-expanding funnel 1708 has been deployed, a portion of thethrombus extraction catheter 104 such as the outer shaft 138 can beinserted into the lumen 1701 of the introducer sheath 102 via the sealedaperture 112 as depicted in FIG. 23-D. In some embodiments, this caninclude providing the thrombus extraction catheter 104 which comprisesthe thrombus extraction device 202. In some embodiments, the thrombusextraction device 202 can be constrained within the outer shaft 138 andcan inserted, together with the outer shaft 138, into the lumen of theelongate member 106 via the sealed aperture 112. In some embodiments,the outer shaft 138 of the thrombus extraction catheter 104 can have adiameter so as to dilate the seal of the sealed aperture 112 such thatthe sealed aperture 112 seals around and seals to the outer shaft 138.

After the outer shaft 138 has been inserted into the lumen 1701 of theintroducer sheath 102, a portion of the thrombus extraction catheter 104can be inserted via the introducer sheath 102 into the blood vessel 2202as depicted in FIG. 23-E. In some embodiments, the distal end 132 of thethrombus extraction catheter 104 can be advanced to a position proximateto the thrombus 2200 and/or to a position proximal to the thrombus 2200.In some embodiments, the insertion and/or advance of the thrombusextraction catheter 104 can be monitored and specifically can befluoroscopically monitored. In some embodiments, the position of one orseveral radiopaque markers, including radiopaque marker 222 of thethrombus extraction catheter 104 can be monitored.

After the portion of the thrombus extraction catheter 104 has beeninserted into the blood vessel 2202, a portion of the thrombusextraction catheter 104 can be distally advanced through the clot 2200as depicted in FIG. 23-F. In some embodiments, this distal advancethrough the clot 2200 can be either with or against the direction ofblood flow. In some embodiments, the portion of the thrombus extractioncatheter 104 distally advanced through the clot 2000 can contain and/orconstrain the thrombus extraction device 202. In some embodiments,distally advancing the portion of the thrombus extraction catheter 104through the clot can include advancing the portion of the thrombusextraction catheter 104 until the radiopaque marker 222, that can befluoroscopically monitored and that can be located at the distal end 218of the inner shaft 200, is distally past the thrombus 2200 and/or aportion of the thrombus 2200.

After the portion of the thrombus extraction catheter 104 is distallyadvanced through the clot 2200, the thrombus extraction device 202 canbe deployed as depicted in FIG. 23-G. In some embodiments, the thrombusextraction device 202 can be deployed by either advancing the thrombusextraction device 202 beyond the distal end 204 of the outer shaft 138or by retracting the outer shaft 138 relative to the thrombus extractiondevice 202 until the thrombus extraction device 202 is beyond the distalend 204 of the outer shaft 138. In some embodiments, the thrombusextraction device can be deployed such that the thrombus extractiondevice 202 is distally past the thrombus 2200 and/or distally past adesired portion of the thrombus 2200.

In some embodiments, the thrombus extraction device is advanced beyondthe distal end 204 of the outer shaft 138 by distally advancing theintermediate shaft 140 with respect to the outer shaft 138. In someembodiments, the intermediate shaft 140 can be distally advanced untilthe lock feature 146 contacts the mating feature 148, and the lockfeature 146 can be mated and/or secured to the mating feature 148 to fixthe relative position of the intermediate shaft 140 with respect to theouter shaft 138.

In some embodiments, the deployment of the thrombus extraction device202 can be monitored, and specifically, the deployment of the thrombusextraction device 202 can be fluoroscopically monitored via, forexample, the radiopaque marker 222 and the radiopaque marker located atone or both of the distal end 204 of the outer sheath 138 and the distalend 212 of the intermediate sheath 140. In some embodiments, thedeployment of the thrombus extraction device 202, and specifically theadvancing of the thrombus extraction device 202 beyond the distal end204 of the outer shaft 138 or retracting the outer shaft 138 relative tothe thrombus extraction device 202 can be ceased based on a position thedistal end 204 of the outer sheath 138 comprising the radiopaque marker(first radiopaque marker) relative to the radiopaque marker 222 locatedon the thrombus extraction device 202 (second radiopaque marker).

After the thrombus extraction device 202 is deployed, the thrombusextraction device 202 can be fully expanded as shown in FIG. 23-H. Insome embodiments, this can include allowing the full expansion of thethrombus extraction device 202 such that the thrombus extraction device202 engages a wall 2220 of the blood vessel 2202. In some embodiments,the thrombus extraction device 202 can be fully expanded by moving theplunger 154 from the first position to the second position and securingthe plunger 154 in the second position to thereby fix the relativeposition of the inner shaft 200 with respect to the intermediate shaft140. In some embodiments, the movement of the plunger 154 from the firstposition to the second position proximally retracts the inner shaft 200with respect to the intermediate shaft 140 to thereby fully expand theexpandable cylindrical portion 208 of the thrombus extraction device202. The proximal retraction of the inner shaft 200 with respect to theintermediate shaft 140 can further bring the stop 702 into engagementwith the ring feature 700 to thereby fully expand the self-expandingcoring element 206. In some embodiments, the securing of the plunger 154in the second position can secure the self-expanding coring element 206and the thrombus extraction device 202 in full expansion via theengagement of the stop 702 with the ring feature 700.

With reference now to FIGS. 24-A and 24-B, alternative embodiments ofthe steps shown in FIGS. 23-G and 23-H are shown. In some embodiments,these alternative embodiments can be performed when the diameter of theblood vessel 2202 containing the thrombus 2200 decreases below a desiredlevel distally beyond the thrombus 2200. In some embodiments, forexample, as the distance from the heart increases, the diameter of theblood vessel 2202 can decrease. In some embodiments, this diameter candecrease to a point that use of the thrombus extraction device 202 mayno longer be possible.

In such an embodiment, an extension sheath 2300, also referred to hereinas a popliteal sheath 2300, can be percutaneously inserted into theblood vessel 2202 through the wall 2220 of the blood vessel 2202 suchthat at least a portion of the extension sheath 2300 extends from thepatient. In some embodiments, the extension sheath 2300 can bepercutaneously inserted into the blood vessel 2202 at a position beforethe blood vessel diameter decreases below a desired value such as, forexample, below 1 mm, 2 mm, 3 mm, 4 mm, 5 mm, 6 mm, 8 mm, 10 mm, or anyother or intermediate value. In some embodiments the extension sheath2300 can be inserted into the blood vessel 2202 via an access site suchas, for example, the popliteal access site.

The thrombus extraction device 202 can be deployed as depicted in FIG.24-A. In some embodiments, the thrombus extraction device 202 can bedeployed by either advancing the thrombus extraction device 202 beyondthe distal end 204 of the outer shaft 138 and into the extension sheath2300 or by advancing the outer shaft 138 containing the thrombusextraction device 202 into the extension sheath and then retracting theouter shaft 138 relative to the thrombus extraction device 202 until thethrombus extraction device 202 is beyond the distal end 204 of the outershaft 138. In some embodiments, the thrombus extraction device can bedeployed such that the thrombus extraction device 202 is distally pastthe thrombus 2200 and/or distally past a desired portion of the thrombus2200. In some embodiments, all or portions of the thrombus extractiondevice can be contained within the extension sheath 2300.

In some embodiments, the outer shaft 138 of the thrombus extractioncatheter 104 can be separable into a first piece and a second piece. Insome embodiments, this separation can occur at a separation point thatcan comprise, for example, any feature configured to allow separation ofthe first and second pieces. These features can include a partial depthslit or score in the outer shaft 138, an overlapping friction fit in theouter shaft 138, or the like. In some embodiments, the separable outershaft 138 can be used in the place of the extension sheath 2300. In suchan embodiment, the outer shaft 138 can exit the blood vessel 2202 viathe access site such that the separable portion extends from inside theblood vessel 2202 to outside of the patient’s body at the access point.In such an embodiment, the separation portion of the outer sheath 138can serve as the extension sheath 2300 and can remain in the accesspoint when the thrombus extraction device 202 is retracted. Thus, thethrombus extraction device 202 can be deployed by securing the positionof the separation portion of the outer sheath 138 and retracting thethrombus extraction device 202 from that separation portion of the outersheath 138.

In some embodiments, the thrombus extraction device can be advancedbeyond the distal end 204 of the outer shaft 138 by distally advancingthe intermediate shaft 140 with respect to the outer shaft 138. In someembodiments, the intermediate shaft 140 can be distally advanced untilthe lock feature 146 contacts the mating feature 148. In someembodiments, the lock feature 146 can be mated and/or secured to themating feature 148 to fix the relative position of the intermediateshaft 140 with respect to the outer shaft 138.

In some embodiments, the deployment of the thrombus extraction device202 can be fluoroscopically monitored, and specifically, the deploymentof the thrombus extraction device 202 can be fluoroscopically monitoredvia, for example, the radiopaque marker 222 and the radiopaque markerlocated at one or both of the distal end 204 of the outer sheath 138 andthe distal end 212 of the intermediate sheath 140. In some embodiments,the deployment of the thrombus extraction device 202, and specificallythe advancing of the thrombus extraction device 202 beyond the distalend 204 of the outer shaft 138 or retracting the outer shaft 138relative to the thrombus extraction device 202 can be seized based on aposition the distal end 204 of the outer sheath 138 comprising theradiopaque marker (first radiopaque marker) relative to the radiopaquemarker 222 located on the thrombus extraction device 202 (secondradiopaque marker).

After the thrombus extraction device 202 is deployed, the thrombusextraction device 202 can be fully expanded as shown in FIG. 24-B. insome embodiments, the thrombus extraction device 202 can be fullyexpanded while all or portions of the thrombus extraction device 202 arecontained in the extension sheath 2300. In such an embodiment, theportions of the thrombus extraction device 202 contained in theextension sheath 2300 can be prevented from reaching full expansion bythe extension sheath 2300. In such an embodiment, the thrombusextraction device 202 can reach full expansion as the thrombusextraction device is proximately retrieved from the extension sheath2300.

In some embodiments, the full expansion of the thrombus extractiondevice 202 can include allowing the expansion of the thrombus extractiondevice 202 such that the thrombus extraction device 202 engages a wall2220 of the blood vessel 2202. In some embodiments, the thrombusextraction device 202 can be fully expanded by moving the plunger 154from the first position to the second position and securing the plunger154 in the second position to thereby fix the relative position of theinner shaft 200 with respect to the intermediate shaft 140. The movementof the plunger 154 from the first position to the second position canproximally retract the inner shaft 200 with respect to the intermediateshaft 140 to thereby expand the expandable cylindrical portion 208 ofthe thrombus extraction device 202. In some embodiments, the proximalretraction of the inner shaft 200 with respect to the intermediate shaft140 can further bring the stop 702 into engagement with the ring feature700 to thereby fully expand the self-expanding coring element 206. Insome embodiments, the securing of the plunger 154 in the second positioncan secure the self-expanding coring element 206 and the thrombusextraction device 202 in full expansion via the engagement of the stop702 with the ring feature 700

In some such embodiments in which the TED 202 is all or wholly containedwithin the extension sheath 2300, the TED 202 can be retracted until theself-expanding coring element 206 is outside of the extension sheath2300, and which point the inner shaft 200 can be decoupled from thedistal end 217 of the expandable cylindrical portion 208 and the plunger154 can be moved from the first position to the second position to bringthe self-expanding coring element 206 to full expansion. The TED 202 canthen be further retracted and the expandable cylindrical portion 208 canbe expanded by progressively recoupling the distal end 217 of theexpandable cylindrical portion 208 with the inner shaft 200 as theexpandable cylindrical portion 208 exits the extension sheath 2300 untilthe expandable cylindrical portion 208 has completely exited theextension sheath 2300 and is at full expansion with the distal end 217of the expandable cylindrical portion 208 recoupled to the inner shaft140. Alternatively, in some embodiments, the distal end 217 of theexpandable cylindrical portion 208 can remain uncoupled to the innershaft 140 until the expandable cylindrical portion 208 has completelyexited the extension sheath 2300. Once the expandable cylindricalportion 208 has completely exited the extension sheath 2300, the distalend 217 of the expandable cylindrical portion 208 can be recoupled tothe inner shaft 200 and the expandable cylindrical portion 208 can beexpanded to full expansion.

With reference now to FIGS. 25-A to 25-H a process for removal ofthrombus 2200 with an expanded thrombus extraction device 202 is shown.In some embodiments, the thrombus 2200 can be removed via the capture ofthe thrombus in the thrombus extraction device 202 via the proximalretraction of the thrombus extraction device 202 through the thrombus2200, which proximal retraction of the thrombus extraction device 202can be, for example, in a direction of blood flow through the bloodvessel 2202 or against the direction of blood flow through the vessel2202. In some embodiments, the proximal retraction of the thrombusextraction device 202 through the thrombus 2200 can result in thecapture of the distal end 2206 of the thrombus 2200 before the captureof the proximal end 2204 of the thrombus 2200.

In some embodiments, the proximal retraction of the thrombus extractiondevice 202 can result in the separation and/or coring of at least aportion of the thrombus 2200 from the wall 2220 of the blood vessel 2202by, for example, the self-expanding coring element 206 and/or the stentportion, and the capture of that separated portion of the thrombus 2200within the expandable cylindrical portion 208. In some embodiments, theexpandable cylindrical portion 208 can be formed of the braided filamentmesh structure that can be, for example, a net-like filament meshstructure. In some embodiments, a portion of the thrombus can becaptured within the expandable cylindrical portion 208 by entering theexpandable cylindrical portion 208 via the mouth 414 of theself-expanding coring element 206 and/or via one or several of theinterstices 404 of the self-expanding coring element 206.

As seen in FIG. 25-A, the distal end 2206 of the thrombus 2200 isseparated and/or cored from the walls 2220 of the blood vessel 2202 bythe self-expanding coring element 206 via the proximal retraction of thethrombus extraction device 202. As seen in FIG. 25-B, the distal end2206 of the thrombus 2200 is captured in the expandable cylindricalportion 208 of the thrombus extraction device by the continued proximalretraction of the thrombus extraction device through the thrombus 2200.The separation and capture and/or coring and capture of further portionsof the thrombus 2200 by the continued proximal retraction of thethrombus extraction device 202 is shown in FIGS. 25-C, 25-D, and 25-E.As seen in FIG. 25-E, the proximal end 2204 of the thrombus 2200 iscored and captured as the thrombus extraction device 202 is proximallyretracted towards the self-expanding funnel 1708.

In some embodiments, the thrombus extraction device 202 can beproximally retracted until a portion of the self-expanding coringelement 206 is contained within the self-expanding funnel 1708 as seenin FIG. 25-F, and specifically until the mouth 414 of the self-expandingcoring element 206 is contained within the self-expanding funnel 1708.In some embodiments, the containment of the mouth 414 within theself-expanding funnel 1708 can be fluoroscopically verified. In someembodiments, the mouth 414 can be determined as wholly contained withinthe self-expanding funnel 1708 via fluoroscopic monitoring based on thealignment/relative positioning of the distal end 212 of the intermediateshaft 140 comprising a radiopaque marker 2450 and/or the radiopaquemarker 222 with respect to the distal end 110 comprising a radiopaquemarker 2452 of the elongate member 106 of the introducer sheath 102.

When the portion of the self-expanding coring element 206 is containedwithin the self-expanding funnel 1708, or specifically when the mouth414 of the self-expanding coring element 206 is wholly contained withinthe self-expanding funnel 1708, the plunger 154 can be unlocked from thesecond position and can be moved from the second position to the firstposition to thereby move the thrombus extraction device 202 from andexpanded configuration to an unexpanded configuration. In someembodiments, the unlocking of the plunger 154 from the second positioncan unlock and/or decouple the inner shaft 200 with respect to theintermediate shaft 140, and the moving of the plunger 154 from thesecond position to the first position can cause the distal advancing ofthe inner shaft 200 relative to the intermediate shaft 140.

In some embodiments, the thrombus extraction device 202 can be collapsedby moving the thrombus extraction device 202 from the expandedconfiguration to the unexpanded configuration prior to withdrawing thethrombus extraction device 202 from the patient’s body so as to compressthe thrombus 2200 captured by the thrombus extraction device 202. Insome embodiments, the compression of the thrombus 2200 by the thrombusextraction device 202 can secure the position of the thrombus within thethrombus extraction device 202 via, in some embodiments, the engagementof one or several of the plurality of circumferential depressions 1000with the thrombus 2200.

After the thrombus extraction device 202 has been collapsed, thethrombus extraction device 202 can be proximally retracted through theself-expanding funnel 1708 and into the elongate member 106 as depictedin FIG. 25-G. In some embodiments, the collapse of the thrombusextraction device 202 and/or the retraction of the thrombus extractiondevice 202 into the self-expanding funnel 1708 and/or the elongatemember can result in the extrusion of all or portions of the thrombus2200 through pores of the expandable cylindrical portion 208 of thethrombus extraction device 202 including, for example, some or all ofthe first plurality of pores 904 and/or the second plurality of pores906. In some embodiments, the all or portions of the thrombus 2200 canbe extruded through some or all of the second plurality of pores 906which can be larger than the first plurality of pores 904. In someembodiments, the pores in the second plurality of pores 906 can be sizedto be sufficiently small such that any thrombus portions of the thrombus2200 extruded through the pores is sufficiently small to have little orno clinical significance. In some embodiments, these extruded all orportions of the thrombus 2200 can be captured by the self-expandingfunnel 1708.

The thrombus extraction device 202 can continue to be proximallyretracted as depicted in FIG. 25-H until the thrombus extraction device202 and the captured thrombus 2200 is fully contained within theelongate member 106. In some embodiments, the seal dilator 170 can beinserted into the sealed aperture 112 and the thrombus extraction device202 and the captured thrombus 2200 can then be withdrawn or removed fromthe patient’s body and from the elongate member 106 via the sealedaperture 112 in the seal dilator 170. In some embodiments, thrombuscaptured by the self-expanding funnel 1708 can then either be guidedinto the elongate member 106 and specifically into the lumen 1701 of theelongate member 106 or further compressed and/or broken up by theself-expanding funnel 1708 and then allowed to pass through theself-expanding funnel 1708, and particularly through the mesh of theself-expanding funnel 1708. In some embodiments, this thrombus can beaspirated through the lumen 1701 of the elongate member 106 and theaspiration port 114. In some embodiments, the aspiration of the thrombusvia the aspiration port 114 can include the opening of the aspirationvalve 118. After the thrombus is captured by the self-expanding funnel1708 has been aspirated, the introducer sheath 102 can be removed fromthe patient’s body.

With reference now to FIGS. 26-28 , introduction techniques foraccessing the thrombus 2200 are shown. In some embodiments, theseintroduction techniques can allow the use of a larger sized introducersheath 102 due to the larger size of the vessels in the path to thethrombus. In some embodiments, this larger size of the introducer sheath102 can ease the removal of thrombus through the introducer sheath 102as, in some embodiments, the size of the lumen 1701 of the introducersheath 102 can increase as the size of the introducer sheath 102increases. Further, in some embodiments, the user of a larger sizedintroducer sheath 102 can allow the removal of larger thrombus. In someembodiments, the lengths of the components of the thrombus extractionsystem 100, and particularly the lengths of the introducer sheath 102and the thrombus extraction catheter 104 can vary based on the selectedtechnique for accessing the thrombus and/or based on the location of thethrombus.

As seen in FIG. 26 , the introducer sheath 102 can be inserted into thepatient’s body via an internal jugular access site 2500. The introducersheath 102 can extend from the internal jugular access site 2500 to thedeployment position 2502 which can be proximal to the thrombus 2200. Inembodiments in which the introducer sheath 102 comprises theself-expanding funnel 1708, the self-expanding funnel 1708 can bedeployed at the deployment position 2502. In the embodiment shown inFIG. 26 , the introducer sheath can extend from the internal jugularaccess site 2500 through the superior vena cava and the inferior venacava to the deployment position 2502 in one of the common iliac veins.In some embodiments, the deployment position 2502 can be located in, forexample, the inferior vena cava, one of the iliac veins, the femoralvein, the popliteal vein, before or beyond the iliac arch, or any otherlocation proximate to and/or proximal to the thrombus 2200. In someembodiments, the use of the internal jugular access site 2500 can allowfor a larger diameter of the elongate member 106.

As seen in FIG. 27 , in some embodiments, use of the internal jugularaccess site 2500 can be combined with use of the extension sheath 2300that can be inserted into the blood vessel 2202 at a popliteal accesssite 2600. In some such embodiments, the thrombus extraction device canwholly or partially exit the patient’s body while contained in theextension sheath 2300 before being retracted through the thrombus 2200.

As seen in FIG. 28 , the introducer sheath can, in some embodiments, beinserted into the patient’s body into an access site connected to theblood vessel 2202 containing the thrombus via the common iliac veins. Inthe specific embodiment shown in FIG. 28 , this can be achieved viainsertion into the patient’s body via a femoral access site 2700. Insome embodiments, use of an access site connected to the blood vessel2202 via the common iliac veins, and specifically user of the femoralaccess site 2700 can be combined with user of the extension sheath 2300that can be inserted into the blood vessel 2202 at a popliteal accesssite 2600. In some such embodiments, the thrombus extraction device canwholly or partially exit the patient’s body while contained in theextension sheath 2300 before being retracted through the thrombus 2200.

Other variations are within the spirit of the present invention. Thus,while the invention is susceptible to various modifications andalternative constructions, certain illustrated embodiments thereof areshown in the drawings and have been described above in detail. It shouldbe understood, however, that there is no intention to limit theinvention to the specific form or forms disclosed, but on the contrary,the intention is to cover all modifications, alternative constructions,and equivalents falling within the spirit and scope of the invention, asdefined in the appended claims.

In the previous description, various embodiments of the presentinvention are described. For purposes of explanation, specificconfigurations and details are set forth in order to provide a thoroughunderstanding of the embodiments. However, it will also be apparent toone skilled in the art that the present invention may be practicedwithout the specific details. Furthermore, well-known features may beomitted or simplified in order not to obscure the embodiment beingdescribed.

The use of the terms “a” and “an” and “the” and similar referents in thecontext of describing the invention (especially in the context of thefollowing claims) are to be construed to cover both the singular and theplural, unless otherwise indicated herein or clearly contradicted bycontext. The terms “comprising,” “having,” “including,” and “containing”are to be construed as open-ended terms (i.e., meaning “including, butnot limited to,”) unless otherwise noted. The term “connected” is to beconstrued as partly or wholly contained within, attached to, or joinedtogether, even if there is something intervening. Recitation of rangesof values herein are merely intended to serve as a shorthand method ofreferring individually to each separate value falling within the range,unless otherwise indicated herein, and each separate value isincorporated into the specification as if it were individually recitedherein. All methods described herein can be performed in any suitableorder unless otherwise indicated herein or otherwise clearlycontradicted by context. The use of any and all examples, or exemplarylanguage (e.g., “such as”) provided herein, is intended merely to betterilluminate embodiments of the invention and does not pose a limitationon the scope of the invention unless otherwise claimed. No language inthe specification should be construed as indicating any non-claimedelement as essential to the practice of the invention.

Preferred embodiments of this invention are described herein, includingthe best mode known to the inventors for carrying out the invention.Variations of those preferred embodiments may become apparent to thoseof ordinary skill in the art upon reading the foregoing description. Theinventors expect skilled artisans to employ such variations asappropriate, and the inventors intend for the invention to be practicedotherwise than as specifically described herein. Accordingly, thisinvention includes all modifications and equivalents of the subjectmatter recited in the claims appended hereto as permitted by applicablelaw. Moreover, any combination of the above-described elements in allpossible variations thereof is encompassed by the invention unlessotherwise indicated herein or otherwise clearly contradicted by context.

All references, including publications, patent applications, andpatents, cited herein are hereby incorporated by reference to the sameextent as if each reference were individually and specifically indicatedto be incorporated by reference and were set forth in its entiretyherein.

What is claimed is:
 1. A clot treatment assembly, comprising: a firstelongate shaft defining a lumen and having a distal portion a proximalportion; a funnel coupled to the distal portion of the first elongateshaft; a hub coupled to the proximal portion of the first elongateshaft; an aspiration source; a fluid path extending from the distalportion of the first elongate shaft, through the lumen of the elongateshaft, through the hub, and to the aspiration source; and a secondelongate shaft coaxial with the first elongate shaft, wherein- thesecond elongate shaft includes a distal portion and a proximal portion,the proximal portion is positioned at least partially within the hub,the second elongate shaft is axially movable relative to the firstelongate shaft between a first position and a second position, in thefirst position, the distal portion of the second elongate shaft extendsover the funnel to radially constrain the funnel in a constrainedconfiguration, and in the second position, the funnel is unconstrainedby the distal portion of the second elongate shaft and configured toself-expand to an expanded configuration.
 2. The clot treatment assemblyof claim 1 wherein the hub includes a seal configured to seal the lumenof the first elongate shaft.
 3. The clot treatment assembly of claim 1wherein the hub includes a self-sealing seal configured to seal thelumen of the first elongate shaft.
 4. The clot treatment assembly ofclaim 1 wherein the hub comprises a stop portion configured to inhibitfurther movement of the second elongate shaft past the second position.5. The clot treatment assembly of claim 1 wherein the hub is shaped andsized to inhibit further movement of the second elongate shaft past thesecond position.
 6. The clot treatment assembly of claim 1, furthercomprising a valve along the fluid path between the aspiration sourceand the lumen of the first elongate shaft, wherein the valve isconfigured to control application of vacuum pressure generated by theaspiration source to the lumen of the elongate shaft.
 7. The clottreatment assembly of claim 6 wherein the valve is user actuatable. 8.The clot treatment assembly of claim 1, further comprising auser-actuatable valve along the fluid path between the aspiration sourceand the lumen of the first elongate shaft, wherein the user-actuatablevalve is movable between (a) a closed position in which the aspirationsource is fluidly disconnected from the lumen of the first elongateshaft and (b) an open position in which the aspiration source is fluidlyconnected to the lumen of the first elongate shaft.
 9. The clottreatment assembly of claim 1 wherein the proximal portion of the firstelongate shaft is fixedly coupled to the hub, and wherein the secondelongate shaft is axially movable relative to the hub.
 10. The clottreatment assembly of claim 1 wherein the funnel extends distally fromthe distal portion of the first elongate shaft.
 11. The clot treatmentassembly of claim 1 wherein the funnel has a conical shape in theexpanded configuration.
 12. The clot treatment assembly of claim 1wherein the funnel extends distally from the distal portion of the firstelongate shaft, wherein the funnel has a conical shape in the expandedconfiguration, and wherein the funnel has a minimum diameter at thedistal portion of the first elongate shaft in the expandedconfiguration.
 13. The clot treatment assembly of claim 1 wherein thefunnel includes a laser cut metal structure defining a plurality ofpores.
 14. The clot treatment assembly of claim 1 wherein the funnelincludes a laser cut nitinol structure defining a plurality of pores.15. The clot treatment assembly of claim 1 wherein the funnel includes alaser cut tube.
 16. The clot treatment assembly of claim 1 wherein thefunnel is impermeable to blood.
 17. A clot treatment assembly,comprising: a first elongate shaft defining a lumen and having a distalportion a proximal portion; a funnel coupled to the distal portion ofthe first elongate shaft; a hub fixedly coupled to the proximal portionof the first elongate shaft, wherein the hub includes a stop portion; anaspiration source; a fluid path extending from the distal portion of thefirst elongate shaft, through the lumen of the elongate shaft, throughthe hub, and to the aspiration source; and a second elongate shaftcoaxial with the first elongate shaft, wherein- the second elongateshaft includes a distal portion and a proximal portion, the secondelongate shaft is axially movable relative to the first elongate shaftin a single direction between a first position and a second position,the stop portion of the hub is configured to inhibit further movement ofthe second elongate shaft in the single direction past the secondposition, in the first position, the distal portion of the secondelongate shaft extends over the funnel to radially constrain the funnelin a constrained configuration, and in the second position, the funnelis unconstrained by the distal portion of the second elongate shaft andconfigured to self-expand to an expanded configuration.
 18. The clottreatment assembly of claim 17, further comprising a user-actuatablevalve along the fluid path between the aspiration source and the lumenof the first elongate shaft, wherein- the user-actuatable valve ismovable between (a) a closed position in which the aspiration source isfluidly disconnected from the lumen of the first elongate shaft and (b)an open position in which the aspiration source is fluidly connected tothe lumen of the first elongate shaft, the proximal portion of the firstelongate shaft is fixedly coupled to the hub, the second elongate shaftis axially movable relative to the hub, and the hub includes a sealconfigured to seal the lumen of the first elongate shaft.
 19. The clottreatment assembly of claim 17 wherein- the funnel includes a laser cutmetal structure defining a plurality of pores, the funnel extendsdistally from the distal portion of the first elongate shaft, and thefunnel has a conical shape in the expanded configuration.
 20. The clottreatment assembly of claim 1 wherein the hub includes a seal configuredto seal the lumen of the first elongate shaft.